Name: rs11378464
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.

rs11378464

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:64664479-64664495 (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(A)₈ / del(A)₇ / del(A)₅ / del(…
del(A)₈ / del(A)₇ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₈=0.0000 (0/8504, ALFA)
del(A)₇=0.0000 (0/8504, ALFA)
delAAA=0.0000 (0/8504, ALFA) (+ 9 more)
delAA=0.0000 (0/8504, ALFA)
delA=0.0000 (0/8504, ALFA)
dupA=0.0000 (0/8504, ALFA)
dupAA=0.0000 (0/8504, ALFA)
dupAAA=0.0000 (0/8504, ALFA)
dup(A)₄=0.0000 (0/8504, ALFA)
dup(A)₅=0.0000 (0/8504, ALFA)
dupA=0.2909 (1457/5008, 1000G)
dupA=0.40 (16/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NRXN2 : 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	HWEP
Total	Global	8504	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	7108	AAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	580	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	22	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	558	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	36	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	30	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	6	AAAAAAAAAAAAAAAAA=1.0	AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	N/A
Latin American 1	Sub	78	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	376	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	66	AAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	260	AAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	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	8504	(A)₁₇=1.0000	del(A)₈=0.0000, del(A)₇=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	European	Sub	7108	(A)₁₇=1.0000	del(A)₈=0.0000, del(A)₇=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000, dup(A)₄=0.0000, dup(A)₅=0.0000
Allele Frequency Aggregator	African	Sub	580	(A)₁₇=1.000	del(A)₈=0.000, del(A)₇=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 2	Sub	376	(A)₁₇=1.000	del(A)₈=0.000, del(A)₇=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Other	Sub	260	(A)₁₇=1.000	del(A)₈=0.000, del(A)₇=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000, dup(A)₄=0.000, dup(A)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	78	(A)₁₇=1.00	del(A)₈=0.00, del(A)₇=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	South Asian	Sub	66	(A)₁₇=1.00	del(A)₈=0.00, del(A)₇=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
Allele Frequency Aggregator	Asian	Sub	36	(A)₁₇=1.00	del(A)₈=0.00, del(A)₇=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00, dup(A)₄=0.00, dup(A)₅=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupA=0.2909
1000Genomes	African	Sub	1322	- No frequency provided	dupA=0.4433
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupA=0.3621
1000Genomes	Europe	Sub	1006	- No frequency provided	dupA=0.1789
1000Genomes	South Asian	Sub	978	- No frequency provided	dupA=0.188
1000Genomes	American	Sub	694	- No frequency provided	dupA=0.205
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupA=0.40

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 11	NC_000011.10:g.64664488_64664495del
GRCh38.p14 chr 11	NC_000011.10:g.64664489_64664495del
GRCh38.p14 chr 11	NC_000011.10:g.64664491_64664495del
GRCh38.p14 chr 11	NC_000011.10:g.64664492_64664495del
GRCh38.p14 chr 11	NC_000011.10:g.64664493_64664495del
GRCh38.p14 chr 11	NC_000011.10:g.64664494_64664495del
GRCh38.p14 chr 11	NC_000011.10:g.64664495del
GRCh38.p14 chr 11	NC_000011.10:g.64664495dup
GRCh38.p14 chr 11	NC_000011.10:g.64664494_64664495dup
GRCh38.p14 chr 11	NC_000011.10:g.64664493_64664495dup
GRCh38.p14 chr 11	NC_000011.10:g.64664492_64664495dup
GRCh38.p14 chr 11	NC_000011.10:g.64664491_64664495dup
GRCh37.p13 chr 11	NC_000011.9:g.64431960_64431967del
GRCh37.p13 chr 11	NC_000011.9:g.64431961_64431967del
GRCh37.p13 chr 11	NC_000011.9:g.64431963_64431967del
GRCh37.p13 chr 11	NC_000011.9:g.64431964_64431967del
GRCh37.p13 chr 11	NC_000011.9:g.64431965_64431967del
GRCh37.p13 chr 11	NC_000011.9:g.64431966_64431967del
GRCh37.p13 chr 11	NC_000011.9:g.64431967del
GRCh37.p13 chr 11	NC_000011.9:g.64431967dup
GRCh37.p13 chr 11	NC_000011.9:g.64431966_64431967dup
GRCh37.p13 chr 11	NC_000011.9:g.64431965_64431967dup
GRCh37.p13 chr 11	NC_000011.9:g.64431964_64431967dup
GRCh37.p13 chr 11	NC_000011.9:g.64431963_64431967dup
NRXN2 RefSeqGene	NG_047107.1:g.63703_63710del
NRXN2 RefSeqGene	NG_047107.1:g.63704_63710del
NRXN2 RefSeqGene	NG_047107.1:g.63706_63710del
NRXN2 RefSeqGene	NG_047107.1:g.63707_63710del
NRXN2 RefSeqGene	NG_047107.1:g.63708_63710del
NRXN2 RefSeqGene	NG_047107.1:g.63709_63710del
NRXN2 RefSeqGene	NG_047107.1:g.63710del
NRXN2 RefSeqGene	NG_047107.1:g.63710dup
NRXN2 RefSeqGene	NG_047107.1:g.63709_63710dup
NRXN2 RefSeqGene	NG_047107.1:g.63708_63710dup
NRXN2 RefSeqGene	NG_047107.1:g.63707_63710dup
NRXN2 RefSeqGene	NG_047107.1:g.63706_63710dup

Gene: NRXN2, neurexin 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NRXN2 transcript variant 4	NM_001376262.1:c.1798+276… NM_001376262.1:c.1798+2764_1798+2771del	N/A	Intron Variant
NRXN2 transcript variant 5	NM_001376263.1:c.1777+276… NM_001376263.1:c.1777+2764_1777+2771del	N/A	Intron Variant
NRXN2 transcript variant 7	NM_001376265.1:c.1753+276… NM_001376265.1:c.1753+2764_1753+2771del	N/A	Intron Variant
NRXN2 transcript variant 6	NM_001376266.1:c.1774+276… NM_001376266.1:c.1774+2764_1774+2771del	N/A	Intron Variant
NRXN2 transcript variant 8	NM_001376267.1:c.1777+276… NM_001376267.1:c.1777+2764_1777+2771del	N/A	Intron Variant
NRXN2 transcript variant alpha-1	NM_015080.4:c.1798+2764_1… NM_015080.4:c.1798+2764_1798+2771del	N/A	Intron Variant
NRXN2 transcript variant alpha-2	NM_138732.3:c.1705+2764_1… NM_138732.3:c.1705+2764_1705+2771del	N/A	Intron Variant
NRXN2 transcript variant 9	NM_001400681.1:c.	N/A	Genic Upstream Transcript Variant
NRXN2 transcript variant 10	NM_001400682.1:c.	N/A	Genic Upstream Transcript Variant
NRXN2 transcript variant beta	NM_138734.3:c.	N/A	Genic Upstream Transcript 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	(A)₁₇=	del(A)₈	del(A)₇	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅
GRCh38.p14 chr 11	NC_000011.10:g.64664479_64664495=	NC_000011.10:g.64664488_64664495del	NC_000011.10:g.64664489_64664495del	NC_000011.10:g.64664491_64664495del	NC_000011.10:g.64664492_64664495del	NC_000011.10:g.64664493_64664495del	NC_000011.10:g.64664494_64664495del	NC_000011.10:g.64664495del	NC_000011.10:g.64664495dup	NC_000011.10:g.64664494_64664495dup	NC_000011.10:g.64664493_64664495dup	NC_000011.10:g.64664492_64664495dup	NC_000011.10:g.64664491_64664495dup
GRCh37.p13 chr 11	NC_000011.9:g.64431951_64431967=	NC_000011.9:g.64431960_64431967del	NC_000011.9:g.64431961_64431967del	NC_000011.9:g.64431963_64431967del	NC_000011.9:g.64431964_64431967del	NC_000011.9:g.64431965_64431967del	NC_000011.9:g.64431966_64431967del	NC_000011.9:g.64431967del	NC_000011.9:g.64431967dup	NC_000011.9:g.64431966_64431967dup	NC_000011.9:g.64431965_64431967dup	NC_000011.9:g.64431964_64431967dup	NC_000011.9:g.64431963_64431967dup
NRXN2 RefSeqGene	NG_047107.1:g.63694_63710=	NG_047107.1:g.63703_63710del	NG_047107.1:g.63704_63710del	NG_047107.1:g.63706_63710del	NG_047107.1:g.63707_63710del	NG_047107.1:g.63708_63710del	NG_047107.1:g.63709_63710del	NG_047107.1:g.63710del	NG_047107.1:g.63710dup	NG_047107.1:g.63709_63710dup	NG_047107.1:g.63708_63710dup	NG_047107.1:g.63707_63710dup	NG_047107.1:g.63706_63710dup
NRXN2 transcript variant 4	NM_001376262.1:c.1798+2771=	NM_001376262.1:c.1798+2764_1798+2771del	NM_001376262.1:c.1798+2765_1798+2771del	NM_001376262.1:c.1798+2767_1798+2771del	NM_001376262.1:c.1798+2768_1798+2771del	NM_001376262.1:c.1798+2769_1798+2771del	NM_001376262.1:c.1798+2770_1798+2771del	NM_001376262.1:c.1798+2771del	NM_001376262.1:c.1798+2771dup	NM_001376262.1:c.1798+2770_1798+2771dup	NM_001376262.1:c.1798+2769_1798+2771dup	NM_001376262.1:c.1798+2768_1798+2771dup	NM_001376262.1:c.1798+2767_1798+2771dup
NRXN2 transcript variant 5	NM_001376263.1:c.1777+2771=	NM_001376263.1:c.1777+2764_1777+2771del	NM_001376263.1:c.1777+2765_1777+2771del	NM_001376263.1:c.1777+2767_1777+2771del	NM_001376263.1:c.1777+2768_1777+2771del	NM_001376263.1:c.1777+2769_1777+2771del	NM_001376263.1:c.1777+2770_1777+2771del	NM_001376263.1:c.1777+2771del	NM_001376263.1:c.1777+2771dup	NM_001376263.1:c.1777+2770_1777+2771dup	NM_001376263.1:c.1777+2769_1777+2771dup	NM_001376263.1:c.1777+2768_1777+2771dup	NM_001376263.1:c.1777+2767_1777+2771dup
NRXN2 transcript variant 7	NM_001376265.1:c.1753+2771=	NM_001376265.1:c.1753+2764_1753+2771del	NM_001376265.1:c.1753+2765_1753+2771del	NM_001376265.1:c.1753+2767_1753+2771del	NM_001376265.1:c.1753+2768_1753+2771del	NM_001376265.1:c.1753+2769_1753+2771del	NM_001376265.1:c.1753+2770_1753+2771del	NM_001376265.1:c.1753+2771del	NM_001376265.1:c.1753+2771dup	NM_001376265.1:c.1753+2770_1753+2771dup	NM_001376265.1:c.1753+2769_1753+2771dup	NM_001376265.1:c.1753+2768_1753+2771dup	NM_001376265.1:c.1753+2767_1753+2771dup
NRXN2 transcript variant 6	NM_001376266.1:c.1774+2771=	NM_001376266.1:c.1774+2764_1774+2771del	NM_001376266.1:c.1774+2765_1774+2771del	NM_001376266.1:c.1774+2767_1774+2771del	NM_001376266.1:c.1774+2768_1774+2771del	NM_001376266.1:c.1774+2769_1774+2771del	NM_001376266.1:c.1774+2770_1774+2771del	NM_001376266.1:c.1774+2771del	NM_001376266.1:c.1774+2771dup	NM_001376266.1:c.1774+2770_1774+2771dup	NM_001376266.1:c.1774+2769_1774+2771dup	NM_001376266.1:c.1774+2768_1774+2771dup	NM_001376266.1:c.1774+2767_1774+2771dup
NRXN2 transcript variant 8	NM_001376267.1:c.1777+2771=	NM_001376267.1:c.1777+2764_1777+2771del	NM_001376267.1:c.1777+2765_1777+2771del	NM_001376267.1:c.1777+2767_1777+2771del	NM_001376267.1:c.1777+2768_1777+2771del	NM_001376267.1:c.1777+2769_1777+2771del	NM_001376267.1:c.1777+2770_1777+2771del	NM_001376267.1:c.1777+2771del	NM_001376267.1:c.1777+2771dup	NM_001376267.1:c.1777+2770_1777+2771dup	NM_001376267.1:c.1777+2769_1777+2771dup	NM_001376267.1:c.1777+2768_1777+2771dup	NM_001376267.1:c.1777+2767_1777+2771dup
NRXN2 transcript variant alpha-1	NM_015080.3:c.1798+2771=	NM_015080.3:c.1798+2764_1798+2771del	NM_015080.3:c.1798+2765_1798+2771del	NM_015080.3:c.1798+2767_1798+2771del	NM_015080.3:c.1798+2768_1798+2771del	NM_015080.3:c.1798+2769_1798+2771del	NM_015080.3:c.1798+2770_1798+2771del	NM_015080.3:c.1798+2771del	NM_015080.3:c.1798+2771dup	NM_015080.3:c.1798+2770_1798+2771dup	NM_015080.3:c.1798+2769_1798+2771dup	NM_015080.3:c.1798+2768_1798+2771dup	NM_015080.3:c.1798+2767_1798+2771dup
NRXN2 transcript variant alpha-1	NM_015080.4:c.1798+2771=	NM_015080.4:c.1798+2764_1798+2771del	NM_015080.4:c.1798+2765_1798+2771del	NM_015080.4:c.1798+2767_1798+2771del	NM_015080.4:c.1798+2768_1798+2771del	NM_015080.4:c.1798+2769_1798+2771del	NM_015080.4:c.1798+2770_1798+2771del	NM_015080.4:c.1798+2771del	NM_015080.4:c.1798+2771dup	NM_015080.4:c.1798+2770_1798+2771dup	NM_015080.4:c.1798+2769_1798+2771dup	NM_015080.4:c.1798+2768_1798+2771dup	NM_015080.4:c.1798+2767_1798+2771dup
NRXN2 transcript variant alpha-2	NM_138732.2:c.1705+2771=	NM_138732.2:c.1705+2764_1705+2771del	NM_138732.2:c.1705+2765_1705+2771del	NM_138732.2:c.1705+2767_1705+2771del	NM_138732.2:c.1705+2768_1705+2771del	NM_138732.2:c.1705+2769_1705+2771del	NM_138732.2:c.1705+2770_1705+2771del	NM_138732.2:c.1705+2771del	NM_138732.2:c.1705+2771dup	NM_138732.2:c.1705+2770_1705+2771dup	NM_138732.2:c.1705+2769_1705+2771dup	NM_138732.2:c.1705+2768_1705+2771dup	NM_138732.2:c.1705+2767_1705+2771dup
NRXN2 transcript variant alpha-2	NM_138732.3:c.1705+2771=	NM_138732.3:c.1705+2764_1705+2771del	NM_138732.3:c.1705+2765_1705+2771del	NM_138732.3:c.1705+2767_1705+2771del	NM_138732.3:c.1705+2768_1705+2771del	NM_138732.3:c.1705+2769_1705+2771del	NM_138732.3:c.1705+2770_1705+2771del	NM_138732.3:c.1705+2771del	NM_138732.3:c.1705+2771dup	NM_138732.3:c.1705+2770_1705+2771dup	NM_138732.3:c.1705+2769_1705+2771dup	NM_138732.3:c.1705+2768_1705+2771dup	NM_138732.3:c.1705+2767_1705+2771dup
NRXN2 transcript variant X1	XM_005274400.1:c.1777+2771=	XM_005274400.1:c.1777+2764_1777+2771del	XM_005274400.1:c.1777+2765_1777+2771del	XM_005274400.1:c.1777+2767_1777+2771del	XM_005274400.1:c.1777+2768_1777+2771del	XM_005274400.1:c.1777+2769_1777+2771del	XM_005274400.1:c.1777+2770_1777+2771del	XM_005274400.1:c.1777+2771del	XM_005274400.1:c.1777+2771dup	XM_005274400.1:c.1777+2770_1777+2771dup	XM_005274400.1:c.1777+2769_1777+2771dup	XM_005274400.1:c.1777+2768_1777+2771dup	XM_005274400.1:c.1777+2767_1777+2771dup
NRXN2 transcript variant X2	XM_005274401.1:c.1777+2771=	XM_005274401.1:c.1777+2764_1777+2771del	XM_005274401.1:c.1777+2765_1777+2771del	XM_005274401.1:c.1777+2767_1777+2771del	XM_005274401.1:c.1777+2768_1777+2771del	XM_005274401.1:c.1777+2769_1777+2771del	XM_005274401.1:c.1777+2770_1777+2771del	XM_005274401.1:c.1777+2771del	XM_005274401.1:c.1777+2771dup	XM_005274401.1:c.1777+2770_1777+2771dup	XM_005274401.1:c.1777+2769_1777+2771dup	XM_005274401.1:c.1777+2768_1777+2771dup	XM_005274401.1:c.1777+2767_1777+2771dup
NRXN2 transcript variant X3	XM_005274402.1:c.1753+2771=	XM_005274402.1:c.1753+2764_1753+2771del	XM_005274402.1:c.1753+2765_1753+2771del	XM_005274402.1:c.1753+2767_1753+2771del	XM_005274402.1:c.1753+2768_1753+2771del	XM_005274402.1:c.1753+2769_1753+2771del	XM_005274402.1:c.1753+2770_1753+2771del	XM_005274402.1:c.1753+2771del	XM_005274402.1:c.1753+2771dup	XM_005274402.1:c.1753+2770_1753+2771dup	XM_005274402.1:c.1753+2769_1753+2771dup	XM_005274402.1:c.1753+2768_1753+2771dup	XM_005274402.1:c.1753+2767_1753+2771dup
NRXN2 transcript variant X4	XM_005274403.1:c.1006+2771=	XM_005274403.1:c.1006+2764_1006+2771del	XM_005274403.1:c.1006+2765_1006+2771del	XM_005274403.1:c.1006+2767_1006+2771del	XM_005274403.1:c.1006+2768_1006+2771del	XM_005274403.1:c.1006+2769_1006+2771del	XM_005274403.1:c.1006+2770_1006+2771del	XM_005274403.1:c.1006+2771del	XM_005274403.1:c.1006+2771dup	XM_005274403.1:c.1006+2770_1006+2771dup	XM_005274403.1:c.1006+2769_1006+2771dup	XM_005274403.1:c.1006+2768_1006+2771dup	XM_005274403.1:c.1006+2767_1006+2771dup
NRXN2 transcript variant X5	XM_005274404.1:c.934+2771=	XM_005274404.1:c.934+2764_934+2771del	XM_005274404.1:c.934+2765_934+2771del	XM_005274404.1:c.934+2767_934+2771del	XM_005274404.1:c.934+2768_934+2771del	XM_005274404.1:c.934+2769_934+2771del	XM_005274404.1:c.934+2770_934+2771del	XM_005274404.1:c.934+2771del	XM_005274404.1:c.934+2771dup	XM_005274404.1:c.934+2770_934+2771dup	XM_005274404.1:c.934+2769_934+2771dup	XM_005274404.1:c.934+2768_934+2771dup	XM_005274404.1:c.934+2767_934+2771dup
NRXN2 transcript variant X6	XM_005274405.1:c.1000+2771=	XM_005274405.1:c.1000+2764_1000+2771del	XM_005274405.1:c.1000+2765_1000+2771del	XM_005274405.1:c.1000+2767_1000+2771del	XM_005274405.1:c.1000+2768_1000+2771del	XM_005274405.1:c.1000+2769_1000+2771del	XM_005274405.1:c.1000+2770_1000+2771del	XM_005274405.1:c.1000+2771del	XM_005274405.1:c.1000+2771dup	XM_005274405.1:c.1000+2770_1000+2771dup	XM_005274405.1:c.1000+2769_1000+2771dup	XM_005274405.1:c.1000+2768_1000+2771dup	XM_005274405.1:c.1000+2767_1000+2771dup

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#.

40 SubSNP, 24 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40007610	Oct 12, 2018 (152)
2	HGSV	ss79951224	Dec 04, 2013 (142)
3	PJP	ss294706922	Oct 12, 2018 (152)
4	PJP	ss294706923	May 09, 2011 (137)
5	1000GENOMES	ss1371023011	Aug 21, 2014 (142)
6	EVA_GENOME_DK	ss1574364999	Apr 01, 2015 (144)
7	SWEGEN	ss3008231418	Nov 08, 2017 (151)
8	MCHAISSO	ss3063695078	Nov 08, 2017 (151)
9	MCHAISSO	ss3065433207	Nov 08, 2017 (151)
10	PACBIO	ss3786975632	Jul 13, 2019 (153)
11	KHV_HUMAN_GENOMES	ss3814740316	Jul 13, 2019 (153)
12	EVA	ss3832670050	Apr 26, 2020 (154)
13	KOGIC	ss3970068531	Apr 26, 2020 (154)
14	KOGIC	ss3970068532	Apr 26, 2020 (154)
15	KOGIC	ss3970068533	Apr 26, 2020 (154)
16	GNOMAD	ss4236520997	Apr 26, 2021 (155)
17	GNOMAD	ss4236520998	Apr 26, 2021 (155)
18	GNOMAD	ss4236520999	Apr 26, 2021 (155)
19	GNOMAD	ss4236521000	Apr 26, 2021 (155)
20	GNOMAD	ss4236521001	Apr 26, 2021 (155)
21	GNOMAD	ss4236521002	Apr 26, 2021 (155)
22	GNOMAD	ss4236521003	Apr 26, 2021 (155)
23	GNOMAD	ss4236521004	Apr 26, 2021 (155)
24	GNOMAD	ss4236521005	Apr 26, 2021 (155)
25	GNOMAD	ss4236521006	Apr 26, 2021 (155)
26	TOPMED	ss4888150257	Apr 26, 2021 (155)
27	TOPMED	ss4888150258	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5202358885	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5202358886	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5202358887	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5287710561	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5287710562	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5287710563	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5482854805	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5482854806	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5482854807	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5750352598	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5750352599	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5750352600	Oct 16, 2022 (156)
40	EVA	ss5850011488	Oct 16, 2022 (156)
41	1000Genomes	NC_000011.9 - 64431951	Oct 12, 2018 (152)
42	The Danish reference pan genome	NC_000011.9 - 64431951	Apr 26, 2020 (154)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 382152324 (NC_000011.10:64664478::A 37604/90952) Row 382152325 (NC_000011.10:64664478::AA 1682/91058) Row 382152326 (NC_000011.10:64664478::AAA 5/91136)...	-	Apr 26, 2021 (155)
53	Korean Genome Project Submission ignored due to conflicting rows: Row 26446532 (NC_000011.10:64664479::A 669/1808) Row 26446533 (NC_000011.10:64664478:A: 87/1808) Row 26446534 (NC_000011.10:64664479::AA 49/1808)	-	Apr 26, 2020 (154)
54	Korean Genome Project Submission ignored due to conflicting rows: Row 26446532 (NC_000011.10:64664479::A 669/1808) Row 26446533 (NC_000011.10:64664478:A: 87/1808) Row 26446534 (NC_000011.10:64664479::AA 49/1808)	-	Apr 26, 2020 (154)
55	Korean Genome Project Submission ignored due to conflicting rows: Row 26446532 (NC_000011.10:64664479::A 669/1808) Row 26446533 (NC_000011.10:64664478:A: 87/1808) Row 26446534 (NC_000011.10:64664479::AA 49/1808)	-	Apr 26, 2020 (154)
56	8.3KJPN Submission ignored due to conflicting rows: Row 60328192 (NC_000011.9:64431950::A 7500/16690) Row 60328193 (NC_000011.9:64431950:A: 65/16690) Row 60328194 (NC_000011.9:64431950::AA 7/16690)	-	Apr 26, 2021 (155)
57	8.3KJPN Submission ignored due to conflicting rows: Row 60328192 (NC_000011.9:64431950::A 7500/16690) Row 60328193 (NC_000011.9:64431950:A: 65/16690) Row 60328194 (NC_000011.9:64431950::AA 7/16690)	-	Apr 26, 2021 (155)
58	8.3KJPN Submission ignored due to conflicting rows: Row 60328192 (NC_000011.9:64431950::A 7500/16690) Row 60328193 (NC_000011.9:64431950:A: 65/16690) Row 60328194 (NC_000011.9:64431950::AA 7/16690)	-	Apr 26, 2021 (155)
59	14KJPN Submission ignored due to conflicting rows: Row 84189702 (NC_000011.10:64664478::A 12940/28258) Row 84189703 (NC_000011.10:64664478:A: 115/28258) Row 84189704 (NC_000011.10:64664478::AA 9/28258)	-	Oct 16, 2022 (156)
60	14KJPN Submission ignored due to conflicting rows: Row 84189702 (NC_000011.10:64664478::A 12940/28258) Row 84189703 (NC_000011.10:64664478:A: 115/28258) Row 84189704 (NC_000011.10:64664478::AA 9/28258)	-	Oct 16, 2022 (156)
61	14KJPN Submission ignored due to conflicting rows: Row 84189702 (NC_000011.10:64664478::A 12940/28258) Row 84189703 (NC_000011.10:64664478:A: 115/28258) Row 84189704 (NC_000011.10:64664478::AA 9/28258)	-	Oct 16, 2022 (156)
62	TopMed Submission ignored due to conflicting rows: Row 103695913 (NC_000011.10:64664478:AAAAAAA: 5/264690) Row 103695914 (NC_000011.10:64664478:AAAAAAAA: 3/264690)	-	Apr 26, 2021 (155)
63	TopMed Submission ignored due to conflicting rows: Row 103695913 (NC_000011.10:64664478:AAAAAAA: 5/264690) Row 103695914 (NC_000011.10:64664478:AAAAAAAA: 3/264690)	-	Apr 26, 2021 (155)
64	ALFA	NC_000011.10 - 64664479	Apr 26, 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)
rs34973516	May 11, 2012 (137)
rs58196742	May 11, 2012 (137)
rs66526925	May 11, 2012 (137)
rs138920860	Sep 17, 2011 (135)
rs397941043	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4888150258	NC_000011.10:64664478:AAAAAAAA:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4236521006, ss4888150257	NC_000011.10:64664478:AAAAAAA:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4236521005	NC_000011.10:64664478:AAAAA:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4236521004	NC_000011.10:64664478:AAAA:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4236521003	NC_000011.10:64664478:AAA:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4236521002	NC_000011.10:64664478:AA:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss3786975632, ss5202358886	NC_000011.9:64431950:A:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3970068532, ss4236521001, ss5287710563, ss5482854806, ss5750352599	NC_000011.10:64664478:A:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss40007610	NT_167190.1:9737745:A:	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss294706922	NC_000011.8:64188527::A	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss294706923	NC_000011.8:64188543::A	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
54140817, 301224, ss1371023011, ss1574364999, ss3008231418, ss3832670050, ss5202358885	NC_000011.9:64431950::A	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3063695078, ss3065433207, ss3814740316, ss4236520997, ss5287710561, ss5482854805, ss5750352598, ss5850011488	NC_000011.10:64664478::A	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3970068531	NC_000011.10:64664479::A	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss79951224	NT_167190.1:9737762::A	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss5202358887	NC_000011.9:64431950::AA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4236520998, ss5287710562, ss5482854807, ss5750352600	NC_000011.10:64664478::AA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3970068533	NC_000011.10:64664479::AA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4236520999	NC_000011.10:64664478::AAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4236521000	NC_000011.10:64664478::AAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
8496863563	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:64664478:AAAAAAAAAAAA… NC_000011.10:64664478:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(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 rs11378464

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
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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

rs11378464