Name: rs58765518
Published: September 21, 2022
License: Open Access

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs58765518

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:52498330-52498349 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₀ / del(T)₇ / del(T)₅ / del…
del(T)₁₀ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.1105 (713/6450, ALFA)
delTTT=0.4327 (2167/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF578 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	6450	TTTTTTTTTTTTTTTTTTTT=0.7687	TTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0933, TTTTTTTTTTTTTTTTTT=0.1105, TTTTTTTTTTTTTTTTTTTTTT=0.0043, TTTTTTTTTTTTTTTTTTT=0.0206, TTTTTTTTTTTTTTTTTTTTT=0.0020, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.812794	0.035714	0.151491	32
European	Sub	6062	TTTTTTTTTTTTTTTTTTTT=0.7544	TTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0988, TTTTTTTTTTTTTTTTTT=0.1176, TTTTTTTTTTTTTTTTTTTTTT=0.0046, TTTTTTTTTTTTTTTTTTT=0.0219, TTTTTTTTTTTTTTTTTTTTT=0.0021, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.797538	0.038625	0.163837	32
African	Sub	228	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	6	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	222	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	24	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	18	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	16	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	42	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	16	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	62	TTTTTTTTTTTTTTTTTTTT=0.95	TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.05, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6450	(T)₂₀=0.7687	del(T)₁₀=0.0000, del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.0933, delTT=0.1105, delT=0.0206, dupT=0.0020, dupTT=0.0043, dupTTT=0.0000, dup(T)₈=0.0005
Allele Frequency Aggregator	European	Sub	6062	(T)₂₀=0.7544	del(T)₁₀=0.0000, del(T)₇=0.0000, del(T)₄=0.0000, delTTT=0.0988, delTT=0.1176, delT=0.0219, dupT=0.0021, dupTT=0.0046, dupTTT=0.0000, dup(T)₈=0.0005
Allele Frequency Aggregator	African	Sub	228	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₇=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Other	Sub	62	(T)₂₀=0.95	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.05, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Latin American 2	Sub	42	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Asian	Sub	24	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	16	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	16	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₇=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₈=0.00
1000Genomes	Global	Study-wide	5008	(T)₂₀=0.5673	delTTT=0.4327
1000Genomes	African	Sub	1322	(T)₂₀=0.4493	delTTT=0.5507
1000Genomes	East Asian	Sub	1008	(T)₂₀=0.4623	delTTT=0.5377
1000Genomes	Europe	Sub	1006	(T)₂₀=0.7346	delTTT=0.2654
1000Genomes	South Asian	Sub	978	(T)₂₀=0.669	delTTT=0.331
1000Genomes	American	Sub	694	(T)₂₀=0.559	delTTT=0.441

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 19	NC_000019.10:g.52498340_52498349del
GRCh38.p14 chr 19	NC_000019.10:g.52498343_52498349del
GRCh38.p14 chr 19	NC_000019.10:g.52498345_52498349del
GRCh38.p14 chr 19	NC_000019.10:g.52498346_52498349del
GRCh38.p14 chr 19	NC_000019.10:g.52498347_52498349del
GRCh38.p14 chr 19	NC_000019.10:g.52498348_52498349del
GRCh38.p14 chr 19	NC_000019.10:g.52498349del
GRCh38.p14 chr 19	NC_000019.10:g.52498349dup
GRCh38.p14 chr 19	NC_000019.10:g.52498348_52498349dup
GRCh38.p14 chr 19	NC_000019.10:g.52498347_52498349dup
GRCh38.p14 chr 19	NC_000019.10:g.52498346_52498349dup
GRCh38.p14 chr 19	NC_000019.10:g.52498345_52498349dup
GRCh38.p14 chr 19	NC_000019.10:g.52498344_52498349dup
GRCh38.p14 chr 19	NC_000019.10:g.52498342_52498349dup
GRCh37.p13 chr 19	NC_000019.9:g.53001593_53001602del
GRCh37.p13 chr 19	NC_000019.9:g.53001596_53001602del
GRCh37.p13 chr 19	NC_000019.9:g.53001598_53001602del
GRCh37.p13 chr 19	NC_000019.9:g.53001599_53001602del
GRCh37.p13 chr 19	NC_000019.9:g.53001600_53001602del
GRCh37.p13 chr 19	NC_000019.9:g.53001601_53001602del
GRCh37.p13 chr 19	NC_000019.9:g.53001602del
GRCh37.p13 chr 19	NC_000019.9:g.53001602dup
GRCh37.p13 chr 19	NC_000019.9:g.53001601_53001602dup
GRCh37.p13 chr 19	NC_000019.9:g.53001600_53001602dup
GRCh37.p13 chr 19	NC_000019.9:g.53001599_53001602dup
GRCh37.p13 chr 19	NC_000019.9:g.53001598_53001602dup
GRCh37.p13 chr 19	NC_000019.9:g.53001597_53001602dup
GRCh37.p13 chr 19	NC_000019.9:g.53001595_53001602dup

Gene: ZNF578, zinc finger protein 578 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF578 transcript variant 1	NM_001099694.2:c.-19-3487… NM_001099694.2:c.-19-3487_-19-3478del	N/A	Intron Variant
ZNF578 transcript variant 2	NM_001366182.2:c.-19-3487… NM_001366182.2:c.-19-3487_-19-3478del	N/A	Intron Variant
ZNF578 transcript variant X1	XM_047438189.1:c.-19-3487… XM_047438189.1:c.-19-3487_-19-3478del	N/A	Intron Variant
ZNF578 transcript variant X2	XM_047438190.1:c.-19-3487… XM_047438190.1:c.-19-3487_-19-3478del	N/A	Intron Variant
ZNF578 transcript variant X3	XM_047438191.1:c.-19-3487… XM_047438191.1:c.-19-3487_-19-3478del	N/A	Intron Variant
ZNF578 transcript variant X4	XM_047438192.1:c.-19-3487… XM_047438192.1:c.-19-3487_-19-3478del	N/A	Intron Variant
ZNF578 transcript variant X5	XM_047438193.1:c.-19-3487… XM_047438193.1:c.-19-3487_-19-3478del	N/A	Intron Variant
ZNF578 transcript variant X6	XM_047438194.1:c.-99-3487… XM_047438194.1:c.-99-3487_-99-3478del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₀=	del(T)₁₀	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₈
GRCh38.p14 chr 19	NC_000019.10:g.52498330_52498349=	NC_000019.10:g.52498340_52498349del	NC_000019.10:g.52498343_52498349del	NC_000019.10:g.52498345_52498349del	NC_000019.10:g.52498346_52498349del	NC_000019.10:g.52498347_52498349del	NC_000019.10:g.52498348_52498349del	NC_000019.10:g.52498349del	NC_000019.10:g.52498349dup	NC_000019.10:g.52498348_52498349dup	NC_000019.10:g.52498347_52498349dup	NC_000019.10:g.52498346_52498349dup	NC_000019.10:g.52498345_52498349dup	NC_000019.10:g.52498344_52498349dup	NC_000019.10:g.52498342_52498349dup
GRCh37.p13 chr 19	NC_000019.9:g.53001583_53001602=	NC_000019.9:g.53001593_53001602del	NC_000019.9:g.53001596_53001602del	NC_000019.9:g.53001598_53001602del	NC_000019.9:g.53001599_53001602del	NC_000019.9:g.53001600_53001602del	NC_000019.9:g.53001601_53001602del	NC_000019.9:g.53001602del	NC_000019.9:g.53001602dup	NC_000019.9:g.53001601_53001602dup	NC_000019.9:g.53001600_53001602dup	NC_000019.9:g.53001599_53001602dup	NC_000019.9:g.53001598_53001602dup	NC_000019.9:g.53001597_53001602dup	NC_000019.9:g.53001595_53001602dup
ZNF578 transcript variant 1	NM_001099694.1:c.-19-3497=	NM_001099694.1:c.-19-3487_-19-3478del	NM_001099694.1:c.-19-3484_-19-3478del	NM_001099694.1:c.-19-3482_-19-3478del	NM_001099694.1:c.-19-3481_-19-3478del	NM_001099694.1:c.-19-3480_-19-3478del	NM_001099694.1:c.-19-3479_-19-3478del	NM_001099694.1:c.-19-3478del	NM_001099694.1:c.-19-3478dup	NM_001099694.1:c.-19-3479_-19-3478dup	NM_001099694.1:c.-19-3480_-19-3478dup	NM_001099694.1:c.-19-3481_-19-3478dup	NM_001099694.1:c.-19-3482_-19-3478dup	NM_001099694.1:c.-19-3483_-19-3478dup	NM_001099694.1:c.-19-3485_-19-3478dup
ZNF578 transcript variant 1	NM_001099694.2:c.-19-3497=	NM_001099694.2:c.-19-3487_-19-3478del	NM_001099694.2:c.-19-3484_-19-3478del	NM_001099694.2:c.-19-3482_-19-3478del	NM_001099694.2:c.-19-3481_-19-3478del	NM_001099694.2:c.-19-3480_-19-3478del	NM_001099694.2:c.-19-3479_-19-3478del	NM_001099694.2:c.-19-3478del	NM_001099694.2:c.-19-3478dup	NM_001099694.2:c.-19-3479_-19-3478dup	NM_001099694.2:c.-19-3480_-19-3478dup	NM_001099694.2:c.-19-3481_-19-3478dup	NM_001099694.2:c.-19-3482_-19-3478dup	NM_001099694.2:c.-19-3483_-19-3478dup	NM_001099694.2:c.-19-3485_-19-3478dup
ZNF578 transcript variant 2	NM_001366182.2:c.-19-3497=	NM_001366182.2:c.-19-3487_-19-3478del	NM_001366182.2:c.-19-3484_-19-3478del	NM_001366182.2:c.-19-3482_-19-3478del	NM_001366182.2:c.-19-3481_-19-3478del	NM_001366182.2:c.-19-3480_-19-3478del	NM_001366182.2:c.-19-3479_-19-3478del	NM_001366182.2:c.-19-3478del	NM_001366182.2:c.-19-3478dup	NM_001366182.2:c.-19-3479_-19-3478dup	NM_001366182.2:c.-19-3480_-19-3478dup	NM_001366182.2:c.-19-3481_-19-3478dup	NM_001366182.2:c.-19-3482_-19-3478dup	NM_001366182.2:c.-19-3483_-19-3478dup	NM_001366182.2:c.-19-3485_-19-3478dup
ZNF578 transcript variant X1	XM_005258527.1:c.-19-3497=	XM_005258527.1:c.-19-3487_-19-3478del	XM_005258527.1:c.-19-3484_-19-3478del	XM_005258527.1:c.-19-3482_-19-3478del	XM_005258527.1:c.-19-3481_-19-3478del	XM_005258527.1:c.-19-3480_-19-3478del	XM_005258527.1:c.-19-3479_-19-3478del	XM_005258527.1:c.-19-3478del	XM_005258527.1:c.-19-3478dup	XM_005258527.1:c.-19-3479_-19-3478dup	XM_005258527.1:c.-19-3480_-19-3478dup	XM_005258527.1:c.-19-3481_-19-3478dup	XM_005258527.1:c.-19-3482_-19-3478dup	XM_005258527.1:c.-19-3483_-19-3478dup	XM_005258527.1:c.-19-3485_-19-3478dup
ZNF578 transcript variant X1	XM_047438189.1:c.-19-3497=	XM_047438189.1:c.-19-3487_-19-3478del	XM_047438189.1:c.-19-3484_-19-3478del	XM_047438189.1:c.-19-3482_-19-3478del	XM_047438189.1:c.-19-3481_-19-3478del	XM_047438189.1:c.-19-3480_-19-3478del	XM_047438189.1:c.-19-3479_-19-3478del	XM_047438189.1:c.-19-3478del	XM_047438189.1:c.-19-3478dup	XM_047438189.1:c.-19-3479_-19-3478dup	XM_047438189.1:c.-19-3480_-19-3478dup	XM_047438189.1:c.-19-3481_-19-3478dup	XM_047438189.1:c.-19-3482_-19-3478dup	XM_047438189.1:c.-19-3483_-19-3478dup	XM_047438189.1:c.-19-3485_-19-3478dup
ZNF578 transcript variant X2	XM_047438190.1:c.-19-3497=	XM_047438190.1:c.-19-3487_-19-3478del	XM_047438190.1:c.-19-3484_-19-3478del	XM_047438190.1:c.-19-3482_-19-3478del	XM_047438190.1:c.-19-3481_-19-3478del	XM_047438190.1:c.-19-3480_-19-3478del	XM_047438190.1:c.-19-3479_-19-3478del	XM_047438190.1:c.-19-3478del	XM_047438190.1:c.-19-3478dup	XM_047438190.1:c.-19-3479_-19-3478dup	XM_047438190.1:c.-19-3480_-19-3478dup	XM_047438190.1:c.-19-3481_-19-3478dup	XM_047438190.1:c.-19-3482_-19-3478dup	XM_047438190.1:c.-19-3483_-19-3478dup	XM_047438190.1:c.-19-3485_-19-3478dup
ZNF578 transcript variant X3	XM_047438191.1:c.-19-3497=	XM_047438191.1:c.-19-3487_-19-3478del	XM_047438191.1:c.-19-3484_-19-3478del	XM_047438191.1:c.-19-3482_-19-3478del	XM_047438191.1:c.-19-3481_-19-3478del	XM_047438191.1:c.-19-3480_-19-3478del	XM_047438191.1:c.-19-3479_-19-3478del	XM_047438191.1:c.-19-3478del	XM_047438191.1:c.-19-3478dup	XM_047438191.1:c.-19-3479_-19-3478dup	XM_047438191.1:c.-19-3480_-19-3478dup	XM_047438191.1:c.-19-3481_-19-3478dup	XM_047438191.1:c.-19-3482_-19-3478dup	XM_047438191.1:c.-19-3483_-19-3478dup	XM_047438191.1:c.-19-3485_-19-3478dup
ZNF578 transcript variant X4	XM_047438192.1:c.-19-3497=	XM_047438192.1:c.-19-3487_-19-3478del	XM_047438192.1:c.-19-3484_-19-3478del	XM_047438192.1:c.-19-3482_-19-3478del	XM_047438192.1:c.-19-3481_-19-3478del	XM_047438192.1:c.-19-3480_-19-3478del	XM_047438192.1:c.-19-3479_-19-3478del	XM_047438192.1:c.-19-3478del	XM_047438192.1:c.-19-3478dup	XM_047438192.1:c.-19-3479_-19-3478dup	XM_047438192.1:c.-19-3480_-19-3478dup	XM_047438192.1:c.-19-3481_-19-3478dup	XM_047438192.1:c.-19-3482_-19-3478dup	XM_047438192.1:c.-19-3483_-19-3478dup	XM_047438192.1:c.-19-3485_-19-3478dup
ZNF578 transcript variant X5	XM_047438193.1:c.-19-3497=	XM_047438193.1:c.-19-3487_-19-3478del	XM_047438193.1:c.-19-3484_-19-3478del	XM_047438193.1:c.-19-3482_-19-3478del	XM_047438193.1:c.-19-3481_-19-3478del	XM_047438193.1:c.-19-3480_-19-3478del	XM_047438193.1:c.-19-3479_-19-3478del	XM_047438193.1:c.-19-3478del	XM_047438193.1:c.-19-3478dup	XM_047438193.1:c.-19-3479_-19-3478dup	XM_047438193.1:c.-19-3480_-19-3478dup	XM_047438193.1:c.-19-3481_-19-3478dup	XM_047438193.1:c.-19-3482_-19-3478dup	XM_047438193.1:c.-19-3483_-19-3478dup	XM_047438193.1:c.-19-3485_-19-3478dup
ZNF578 transcript variant X6	XM_047438194.1:c.-99-3497=	XM_047438194.1:c.-99-3487_-99-3478del	XM_047438194.1:c.-99-3484_-99-3478del	XM_047438194.1:c.-99-3482_-99-3478del	XM_047438194.1:c.-99-3481_-99-3478del	XM_047438194.1:c.-99-3480_-99-3478del	XM_047438194.1:c.-99-3479_-99-3478del	XM_047438194.1:c.-99-3478del	XM_047438194.1:c.-99-3478dup	XM_047438194.1:c.-99-3479_-99-3478dup	XM_047438194.1:c.-99-3480_-99-3478dup	XM_047438194.1:c.-99-3481_-99-3478dup	XM_047438194.1:c.-99-3482_-99-3478dup	XM_047438194.1:c.-99-3483_-99-3478dup	XM_047438194.1:c.-99-3485_-99-3478dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

58 SubSNP, 35 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81782468	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss96282680	Feb 05, 2009 (130)
3	PJP	ss294966938	May 09, 2011 (135)
4	1000GENOMES	ss1378248538	Aug 21, 2014 (142)
5	EVA_UK10K_ALSPAC	ss1709243587	Apr 01, 2015 (144)
6	EVA_UK10K_TWINSUK	ss1709243701	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1710798151	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1710798152	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710798153	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710798154	Apr 01, 2015 (144)
11	SWEGEN	ss3017645654	Nov 08, 2017 (151)
12	MCHAISSO	ss3064769337	Nov 08, 2017 (151)
13	EVA_DECODE	ss3702968916	Jul 13, 2019 (153)
14	EVA_DECODE	ss3702968918	Jul 13, 2019 (153)
15	EVA_DECODE	ss3702968919	Jul 13, 2019 (153)
16	EVA_DECODE	ss3702968920	Jul 13, 2019 (153)
17	EVA_DECODE	ss3702968921	Jul 13, 2019 (153)
18	ACPOP	ss3743126942	Jul 13, 2019 (153)
19	ACPOP	ss3743126943	Jul 13, 2019 (153)
20	KHV_HUMAN_GENOMES	ss3821432292	Jul 13, 2019 (153)
21	EVA	ss3835514370	Apr 27, 2020 (154)
22	GNOMAD	ss4332948235	Apr 27, 2021 (155)
23	GNOMAD	ss4332948240	Apr 27, 2021 (155)
24	GNOMAD	ss4332948241	Apr 27, 2021 (155)
25	GNOMAD	ss4332948242	Apr 27, 2021 (155)
26	GNOMAD	ss4332948243	Apr 27, 2021 (155)
27	GNOMAD	ss4332948244	Apr 27, 2021 (155)
28	GNOMAD	ss4332948245	Apr 27, 2021 (155)
29	GNOMAD	ss4332948246	Apr 27, 2021 (155)
30	GNOMAD	ss4332948247	Apr 27, 2021 (155)
31	GNOMAD	ss4332948248	Apr 27, 2021 (155)
32	GNOMAD	ss4332948249	Apr 27, 2021 (155)
33	GNOMAD	ss4332948250	Apr 27, 2021 (155)
34	GNOMAD	ss4332948251	Apr 27, 2021 (155)
35	GNOMAD	ss4332948252	Apr 27, 2021 (155)
36	TOMMO_GENOMICS	ss5228244066	Apr 27, 2021 (155)
37	TOMMO_GENOMICS	ss5228244067	Apr 27, 2021 (155)
38	TOMMO_GENOMICS	ss5228244068	Apr 27, 2021 (155)
39	TOMMO_GENOMICS	ss5228244069	Apr 27, 2021 (155)
40	TOMMO_GENOMICS	ss5228244070	Apr 27, 2021 (155)
41	TOMMO_GENOMICS	ss5228244071	Apr 27, 2021 (155)
42	1000G_HIGH_COVERAGE	ss5307618324	Oct 13, 2022 (156)
43	1000G_HIGH_COVERAGE	ss5307618325	Oct 13, 2022 (156)
44	1000G_HIGH_COVERAGE	ss5307618326	Oct 13, 2022 (156)
45	1000G_HIGH_COVERAGE	ss5307618328	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5500081076	Oct 13, 2022 (156)
47	HUGCELL_USP	ss5500081077	Oct 13, 2022 (156)
48	HUGCELL_USP	ss5500081078	Oct 13, 2022 (156)
49	HUGCELL_USP	ss5500081079	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5787041498	Oct 13, 2022 (156)
51	TOMMO_GENOMICS	ss5787041499	Oct 13, 2022 (156)
52	TOMMO_GENOMICS	ss5787041500	Oct 13, 2022 (156)
53	TOMMO_GENOMICS	ss5787041501	Oct 13, 2022 (156)
54	TOMMO_GENOMICS	ss5787041502	Oct 13, 2022 (156)
55	TOMMO_GENOMICS	ss5787041503	Oct 13, 2022 (156)
56	EVA	ss5840691440	Oct 13, 2022 (156)
57	EVA	ss5840691441	Oct 13, 2022 (156)
58	EVA	ss5840691442	Oct 13, 2022 (156)
59	1000Genomes	NC_000019.9 - 53001583	Oct 12, 2018 (152)
60	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 42618452 (NC_000019.9:53001582:TTTT: 211/3854) Row 42618454 (NC_000019.9:53001583:TT: 1393/3854)	-	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 42618452 (NC_000019.9:53001582:TTTT: 211/3854) Row 42618454 (NC_000019.9:53001583:TT: 1393/3854)	-	Oct 12, 2018 (152)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542898185 (NC_000019.10:52498329::T 750/104256) Row 542898190 (NC_000019.10:52498329::TT 111/104250) Row 542898191 (NC_000019.10:52498329::TTT 19/104296)...	-	Apr 27, 2021 (155)
76	Northern Sweden Submission ignored due to conflicting rows: Row 16411807 (NC_000019.9:53001582:TTT: 42/564) Row 16411808 (NC_000019.9:53001582:TT: 75/564)	-	Jul 13, 2019 (153)
77	Northern Sweden Submission ignored due to conflicting rows: Row 16411807 (NC_000019.9:53001582:TTT: 42/564) Row 16411808 (NC_000019.9:53001582:TT: 75/564)	-	Jul 13, 2019 (153)
78	8.3KJPN Submission ignored due to conflicting rows: Row 86213373 (NC_000019.9:53001582:TTT: 6810/16436) Row 86213374 (NC_000019.9:53001582:TT: 600/16436) Row 86213375 (NC_000019.9:53001582::TT 150/16436)...	-	Apr 27, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 86213373 (NC_000019.9:53001582:TTT: 6810/16436) Row 86213374 (NC_000019.9:53001582:TT: 600/16436) Row 86213375 (NC_000019.9:53001582::TT 150/16436)...	-	Apr 27, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 86213373 (NC_000019.9:53001582:TTT: 6810/16436) Row 86213374 (NC_000019.9:53001582:TT: 600/16436) Row 86213375 (NC_000019.9:53001582::TT 150/16436)...	-	Apr 27, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 86213373 (NC_000019.9:53001582:TTT: 6810/16436) Row 86213374 (NC_000019.9:53001582:TT: 600/16436) Row 86213375 (NC_000019.9:53001582::TT 150/16436)...	-	Apr 27, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 86213373 (NC_000019.9:53001582:TTT: 6810/16436) Row 86213374 (NC_000019.9:53001582:TT: 600/16436) Row 86213375 (NC_000019.9:53001582::TT 150/16436)...	-	Apr 27, 2021 (155)
83	8.3KJPN Submission ignored due to conflicting rows: Row 86213373 (NC_000019.9:53001582:TTT: 6810/16436) Row 86213374 (NC_000019.9:53001582:TT: 600/16436) Row 86213375 (NC_000019.9:53001582::TT 150/16436)...	-	Apr 27, 2021 (155)
84	14KJPN Submission ignored due to conflicting rows: Row 120878602 (NC_000019.10:52498329:TTT: 12480/27692) Row 120878603 (NC_000019.10:52498329:TT: 1062/27692) Row 120878604 (NC_000019.10:52498329:TTTT: 41/27692)...	-	Oct 13, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 120878602 (NC_000019.10:52498329:TTT: 12480/27692) Row 120878603 (NC_000019.10:52498329:TT: 1062/27692) Row 120878604 (NC_000019.10:52498329:TTTT: 41/27692)...	-	Oct 13, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 120878602 (NC_000019.10:52498329:TTT: 12480/27692) Row 120878603 (NC_000019.10:52498329:TT: 1062/27692) Row 120878604 (NC_000019.10:52498329:TTTT: 41/27692)...	-	Oct 13, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 120878602 (NC_000019.10:52498329:TTT: 12480/27692) Row 120878603 (NC_000019.10:52498329:TT: 1062/27692) Row 120878604 (NC_000019.10:52498329:TTTT: 41/27692)...	-	Oct 13, 2022 (156)
88	14KJPN Submission ignored due to conflicting rows: Row 120878602 (NC_000019.10:52498329:TTT: 12480/27692) Row 120878603 (NC_000019.10:52498329:TT: 1062/27692) Row 120878604 (NC_000019.10:52498329:TTTT: 41/27692)...	-	Oct 13, 2022 (156)
89	14KJPN Submission ignored due to conflicting rows: Row 120878602 (NC_000019.10:52498329:TTT: 12480/27692) Row 120878603 (NC_000019.10:52498329:TT: 1062/27692) Row 120878604 (NC_000019.10:52498329:TTTT: 41/27692)...	-	Oct 13, 2022 (156)
90	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42618452 (NC_000019.9:53001582:TTTT: 205/3708) Row 42618454 (NC_000019.9:53001583:TT: 1350/3708)	-	Oct 12, 2018 (152)
91	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42618452 (NC_000019.9:53001582:TTTT: 205/3708) Row 42618453 (NC_000019.9:53001584:TT: 1076/3708) Row 42618454 (NC_000019.9:53001583:TTT: 1350/3708)	-	Apr 27, 2020 (154)
92	UK 10K study - Twins Submission ignored due to conflicting rows: Row 42618452 (NC_000019.9:53001582:TTTT: 205/3708) Row 42618454 (NC_000019.9:53001583:TT: 1350/3708)	-	Oct 12, 2018 (152)
93	ALFA	NC_000019.10 - 52498330	Apr 27, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs149361600	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4332948252	NC_000019.10:52498329:TTTTTTTTTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4332948251	NC_000019.10:52498329:TTTTTTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4332948250	NC_000019.10:52498329:TTTTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss1709243587, ss1709243701, ss5228244071, ss5840691442	NC_000019.9:53001582:TTTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3702968916, ss4332948249, ss5787041500	NC_000019.10:52498329:TTTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss81782468, ss294966938	NC_000019.8:57693411:TTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
76980990, ss1378248538, ss3017645654, ss3743126942, ss3835514370, ss5228244066, ss5840691440	NC_000019.9:53001582:TTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss1710798153, ss1710798154	NC_000019.9:53001583:TTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3064769337, ss3821432292, ss4332948248, ss5307618324, ss5500081076, ss5787041498	NC_000019.10:52498329:TTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3702968918	NC_000019.10:52498330:TTT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3743126943, ss5228244067, ss5840691441	NC_000019.9:53001582:TT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
	NC_000019.9:53001583:TT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1710798151, ss1710798152	NC_000019.9:53001584:TT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4332948247, ss5307618328, ss5500081077, ss5787041499	NC_000019.10:52498329:TT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3702968919	NC_000019.10:52498331:TT:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5228244070	NC_000019.9:53001582:T:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4332948246, ss5307618325, ss5500081078, ss5787041503	NC_000019.10:52498329:T:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3702968920	NC_000019.10:52498332:T:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss96282680	NT_011109.16:25269819:T:	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5228244069	NC_000019.9:53001582::T	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4332948235, ss5307618326, ss5500081079, ss5787041502	NC_000019.10:52498329::T	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3702968921	NC_000019.10:52498333::T	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5228244068	NC_000019.9:53001582::TT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332948240, ss5787041501	NC_000019.10:52498329::TT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss96282680	NT_011109.16:25269819:T:TTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332948241	NC_000019.10:52498329::TTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332948242	NC_000019.10:52498329::TTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332948243	NC_000019.10:52498329::TTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332948244	NC_000019.10:52498329::TTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332948245	NC_000019.10:52498329::TTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
1029310122	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:52498329:TTTTTTTTTTTT… NC_000019.10:52498329:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs58765518

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Choose placement

dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs58765518