Name: rs36121550
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.

rs36121550

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:149403003-149403025 (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)₁₄ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₈ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₇
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₄=0.0000 (0/2940, ALFA)
del(A)₁₃=0.0000 (0/2940, ALFA)
del(A)₁₂=0.0000 (0/2940, ALFA) (+ 11 more)
del(A)₁₁=0.0000 (0/2940, ALFA)
del(A)₁₀=0.0000 (0/2940, ALFA)
del(A)₈=0.0000 (0/2940, ALFA)
del(A)₆=0.0000 (0/2940, ALFA)
del(A)₅=0.0000 (0/2940, ALFA)
del(A)₄=0.0000 (0/2940, ALFA)
delAAA=0.0000 (0/2940, ALFA)
delAA=0.0000 (0/2940, ALFA)
delA=0.0000 (0/2940, ALFA)
dupA=0.0000 (0/2940, ALFA)
dupAA=0.0000 (0/2940, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IL17B : 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	2940	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	1918	AAAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	442	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	12	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	430	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	92	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	74	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	18	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	26	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 2	Sub	248	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	46	AAAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	168	AAAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	2940	(A)₂₃=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	European	Sub	1918	(A)₂₃=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₈=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000
Allele Frequency Aggregator	African	Sub	442	(A)₂₃=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	248	(A)₂₃=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Other	Sub	168	(A)₂₃=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₈=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000
Allele Frequency Aggregator	Asian	Sub	92	(A)₂₃=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	South Asian	Sub	46	(A)₂₃=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00
Allele Frequency Aggregator	Latin American 1	Sub	26	(A)₂₃=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₈=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00

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 5	NC_000005.10:g.149403012_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403013_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403014_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403015_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403016_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403018_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403020_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403021_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403022_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403023_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403024_149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403025del
GRCh38.p14 chr 5	NC_000005.10:g.149403025dup
GRCh38.p14 chr 5	NC_000005.10:g.149403024_149403025dup
GRCh38.p14 chr 5	NC_000005.10:g.149403023_149403025dup
GRCh38.p14 chr 5	NC_000005.10:g.149403022_149403025dup
GRCh38.p14 chr 5	NC_000005.10:g.149403019_149403025dup
GRCh37.p13 chr 5	NC_000005.9:g.148782575_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782576_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782577_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782578_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782579_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782581_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782583_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782584_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782585_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782586_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782587_148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782588del
GRCh37.p13 chr 5	NC_000005.9:g.148782588dup
GRCh37.p13 chr 5	NC_000005.9:g.148782587_148782588dup
GRCh37.p13 chr 5	NC_000005.9:g.148782586_148782588dup
GRCh37.p13 chr 5	NC_000005.9:g.148782585_148782588dup
GRCh37.p13 chr 5	NC_000005.9:g.148782582_148782588dup

Gene: IL17B, interleukin 17B (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IL17B transcript variant 2	NM_001317987.2:c.-136+109… NM_001317987.2:c.-136+1092_-136+1105del	N/A	Intron Variant
IL17B transcript variant 1	NM_014443.3:c.	N/A	Genic Upstream Transcript Variant
IL17B transcript variant X2	XM_017009347.2:c.-407+109… XM_017009347.2:c.-407+1092_-407+1105del	N/A	Intron Variant
IL17B transcript variant X3	XM_017009348.2:c.-246+109… XM_017009348.2:c.-246+1092_-246+1105del	N/A	Intron Variant
IL17B transcript variant X1	XM_017009346.2:c.	N/A	Genic Upstream Transcript Variant
IL17B transcript variant X4	XM_047417104.1: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)₂₃=	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₈	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₇
GRCh38.p14 chr 5	NC_000005.10:g.149403003_149403025=	NC_000005.10:g.149403012_149403025del	NC_000005.10:g.149403013_149403025del	NC_000005.10:g.149403014_149403025del	NC_000005.10:g.149403015_149403025del	NC_000005.10:g.149403016_149403025del	NC_000005.10:g.149403018_149403025del	NC_000005.10:g.149403020_149403025del	NC_000005.10:g.149403021_149403025del	NC_000005.10:g.149403022_149403025del	NC_000005.10:g.149403023_149403025del	NC_000005.10:g.149403024_149403025del	NC_000005.10:g.149403025del	NC_000005.10:g.149403025dup	NC_000005.10:g.149403024_149403025dup	NC_000005.10:g.149403023_149403025dup	NC_000005.10:g.149403022_149403025dup	NC_000005.10:g.149403019_149403025dup
GRCh37.p13 chr 5	NC_000005.9:g.148782566_148782588=	NC_000005.9:g.148782575_148782588del	NC_000005.9:g.148782576_148782588del	NC_000005.9:g.148782577_148782588del	NC_000005.9:g.148782578_148782588del	NC_000005.9:g.148782579_148782588del	NC_000005.9:g.148782581_148782588del	NC_000005.9:g.148782583_148782588del	NC_000005.9:g.148782584_148782588del	NC_000005.9:g.148782585_148782588del	NC_000005.9:g.148782586_148782588del	NC_000005.9:g.148782587_148782588del	NC_000005.9:g.148782588del	NC_000005.9:g.148782588dup	NC_000005.9:g.148782587_148782588dup	NC_000005.9:g.148782586_148782588dup	NC_000005.9:g.148782585_148782588dup	NC_000005.9:g.148782582_148782588dup
IL17B transcript variant 2	NM_001317987.2:c.-136+1105=	NM_001317987.2:c.-136+1092_-136+1105del	NM_001317987.2:c.-136+1093_-136+1105del	NM_001317987.2:c.-136+1094_-136+1105del	NM_001317987.2:c.-136+1095_-136+1105del	NM_001317987.2:c.-136+1096_-136+1105del	NM_001317987.2:c.-136+1098_-136+1105del	NM_001317987.2:c.-136+1100_-136+1105del	NM_001317987.2:c.-136+1101_-136+1105del	NM_001317987.2:c.-136+1102_-136+1105del	NM_001317987.2:c.-136+1103_-136+1105del	NM_001317987.2:c.-136+1104_-136+1105del	NM_001317987.2:c.-136+1105del	NM_001317987.2:c.-136+1105dup	NM_001317987.2:c.-136+1104_-136+1105dup	NM_001317987.2:c.-136+1103_-136+1105dup	NM_001317987.2:c.-136+1102_-136+1105dup	NM_001317987.2:c.-136+1099_-136+1105dup
IL17B transcript variant X2	XM_017009347.2:c.-407+1105=	XM_017009347.2:c.-407+1092_-407+1105del	XM_017009347.2:c.-407+1093_-407+1105del	XM_017009347.2:c.-407+1094_-407+1105del	XM_017009347.2:c.-407+1095_-407+1105del	XM_017009347.2:c.-407+1096_-407+1105del	XM_017009347.2:c.-407+1098_-407+1105del	XM_017009347.2:c.-407+1100_-407+1105del	XM_017009347.2:c.-407+1101_-407+1105del	XM_017009347.2:c.-407+1102_-407+1105del	XM_017009347.2:c.-407+1103_-407+1105del	XM_017009347.2:c.-407+1104_-407+1105del	XM_017009347.2:c.-407+1105del	XM_017009347.2:c.-407+1105dup	XM_017009347.2:c.-407+1104_-407+1105dup	XM_017009347.2:c.-407+1103_-407+1105dup	XM_017009347.2:c.-407+1102_-407+1105dup	XM_017009347.2:c.-407+1099_-407+1105dup
IL17B transcript variant X3	XM_017009348.2:c.-246+1105=	XM_017009348.2:c.-246+1092_-246+1105del	XM_017009348.2:c.-246+1093_-246+1105del	XM_017009348.2:c.-246+1094_-246+1105del	XM_017009348.2:c.-246+1095_-246+1105del	XM_017009348.2:c.-246+1096_-246+1105del	XM_017009348.2:c.-246+1098_-246+1105del	XM_017009348.2:c.-246+1100_-246+1105del	XM_017009348.2:c.-246+1101_-246+1105del	XM_017009348.2:c.-246+1102_-246+1105del	XM_017009348.2:c.-246+1103_-246+1105del	XM_017009348.2:c.-246+1104_-246+1105del	XM_017009348.2:c.-246+1105del	XM_017009348.2:c.-246+1105dup	XM_017009348.2:c.-246+1104_-246+1105dup	XM_017009348.2:c.-246+1103_-246+1105dup	XM_017009348.2:c.-246+1102_-246+1105dup	XM_017009348.2:c.-246+1099_-246+1105dup

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#.

33 SubSNP, 21 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42538038	Mar 15, 2006 (126)
2	EVA_DECODE	ss3715937955	Jul 13, 2019 (153)
3	EVA_DECODE	ss3715937956	Jul 13, 2019 (153)
4	EVA_DECODE	ss3715937957	Jul 13, 2019 (153)
5	EVA_DECODE	ss3715937958	Jul 13, 2019 (153)
6	GNOMAD	ss4131532111	Apr 26, 2021 (155)
7	GNOMAD	ss4131532112	Apr 26, 2021 (155)
8	GNOMAD	ss4131532113	Apr 26, 2021 (155)
9	GNOMAD	ss4131532114	Apr 26, 2021 (155)
10	GNOMAD	ss4131532115	Apr 26, 2021 (155)
11	GNOMAD	ss4131532116	Apr 26, 2021 (155)
12	GNOMAD	ss4131532117	Apr 26, 2021 (155)
13	GNOMAD	ss4131532118	Apr 26, 2021 (155)
14	GNOMAD	ss4131532119	Apr 26, 2021 (155)
15	GNOMAD	ss4131532120	Apr 26, 2021 (155)
16	GNOMAD	ss4131532121	Apr 26, 2021 (155)
17	GNOMAD	ss4131532122	Apr 26, 2021 (155)
18	GNOMAD	ss4131532123	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5174699731	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5174699732	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5174699733	Apr 26, 2021 (155)
22	1000G_HIGH_COVERAGE	ss5266273946	Oct 13, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5266273947	Oct 13, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5266273948	Oct 13, 2022 (156)
25	1000G_HIGH_COVERAGE	ss5266273949	Oct 13, 2022 (156)
26	HUGCELL_USP	ss5464194512	Oct 13, 2022 (156)
27	HUGCELL_USP	ss5464194513	Oct 13, 2022 (156)
28	HUGCELL_USP	ss5464194514	Oct 13, 2022 (156)
29	HUGCELL_USP	ss5464194515	Oct 13, 2022 (156)
30	TOMMO_GENOMICS	ss5711940493	Oct 13, 2022 (156)
31	TOMMO_GENOMICS	ss5711940494	Oct 13, 2022 (156)
32	TOMMO_GENOMICS	ss5711940495	Oct 13, 2022 (156)
33	TOMMO_GENOMICS	ss5711940497	Oct 13, 2022 (156)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 207996784 (NC_000005.10:149403002::A 637/57182) Row 207996785 (NC_000005.10:149403002::AA 14/57302) Row 207996786 (NC_000005.10:149403002::AAA 3/57328)...	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 32669038 (NC_000005.9:148782565:A: 130/16486) Row 32669039 (NC_000005.9:148782565::A 37/16486) Row 32669040 (NC_000005.9:148782565:AA: 40/16486)	-	Apr 26, 2021 (155)
48	8.3KJPN Submission ignored due to conflicting rows: Row 32669038 (NC_000005.9:148782565:A: 130/16486) Row 32669039 (NC_000005.9:148782565::A 37/16486) Row 32669040 (NC_000005.9:148782565:AA: 40/16486)	-	Apr 26, 2021 (155)
49	8.3KJPN Submission ignored due to conflicting rows: Row 32669038 (NC_000005.9:148782565:A: 130/16486) Row 32669039 (NC_000005.9:148782565::A 37/16486) Row 32669040 (NC_000005.9:148782565:AA: 40/16486)	-	Apr 26, 2021 (155)
50	14KJPN Submission ignored due to conflicting rows: Row 45777597 (NC_000005.10:149403002:A: 392/28036) Row 45777598 (NC_000005.10:149403002:AA: 121/28036) Row 45777599 (NC_000005.10:149403002::A 132/28036)...	-	Oct 13, 2022 (156)
51	14KJPN Submission ignored due to conflicting rows: Row 45777597 (NC_000005.10:149403002:A: 392/28036) Row 45777598 (NC_000005.10:149403002:AA: 121/28036) Row 45777599 (NC_000005.10:149403002::A 132/28036)...	-	Oct 13, 2022 (156)
52	14KJPN Submission ignored due to conflicting rows: Row 45777597 (NC_000005.10:149403002:A: 392/28036) Row 45777598 (NC_000005.10:149403002:AA: 121/28036) Row 45777599 (NC_000005.10:149403002::A 132/28036)...	-	Oct 13, 2022 (156)
53	14KJPN Submission ignored due to conflicting rows: Row 45777597 (NC_000005.10:149403002:A: 392/28036) Row 45777598 (NC_000005.10:149403002:AA: 121/28036) Row 45777599 (NC_000005.10:149403002::A 132/28036)...	-	Oct 13, 2022 (156)
54	ALFA	NC_000005.10 - 149403003	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4131532123	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4131532122	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4131532121, ss5266273949, ss5464194515	NC_000005.10:149403002:AAAAAAAAAAA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss4131532120	NC_000005.10:149403002:AAAAAAAA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss4131532119	NC_000005.10:149403002:AAAAA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4131532118	NC_000005.10:149403002:AAAA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3715937958, ss4131532117, ss5266273947	NC_000005.10:149403002:AAA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5174699733	NC_000005.9:148782565:AA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532116, ss5266273946, ss5464194514, ss5711940494	NC_000005.10:149403002:AA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3715937957	NC_000005.10:149403003:AA:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5174699731	NC_000005.9:148782565:A:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5464194512, ss5711940493	NC_000005.10:149403002:A:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3715937956	NC_000005.10:149403004:A:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss42538038	NT_029289.11:9945514:A:	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5174699732	NC_000005.9:148782565::A	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532111, ss5266273948, ss5464194513, ss5711940495	NC_000005.10:149403002::A	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3715937955	NC_000005.10:149403005::A	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532112, ss5711940497	NC_000005.10:149403002::AA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
2441824221	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532113	NC_000005.10:149403002::AAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532114	NC_000005.10:149403002::AAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4131532115	NC_000005.10:149403002::AAAAAAA	NC_000005.10:149403002:AAAAAAAAAAA… NC_000005.10:149403002:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(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 rs36121550

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

rs36121550