SNP Links for Gene (Select 8590) - SNP

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Select item 14886173381.

rs1488617338 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:6797717 (GRCh38)
11:6818948 (GRCh37)
Canonical SPDI:: NC_000011.10:6797716:T:C
Gene:: OR6A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.6797717T>C, NC_000011.9:g.6818948T>C

Select item 14885437452.

rs1488543745 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 11:6796469 (GRCh38)
11:6817700 (GRCh37)
Canonical SPDI:: NC_000011.10:6796468:G:A,NC_000011.10:6796468:G:C,NC_000011.10:6796468:G:T
Gene:: OR6A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.6796469G>A, NC_000011.10:g.6796469G>C, NC_000011.10:g.6796469G>T, NC_000011.9:g.6817700G>A, NC_000011.9:g.6817700G>C, NC_000011.9:g.6817700G>T

Select item 14867863993.

rs1486786399 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:6795253 (GRCh38)
11:6816484 (GRCh37)
Canonical SPDI:: NC_000011.10:6795252:G:C
Gene:: OR6A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6795253G>C, NC_000011.9:g.6816484G>C, NM_003696.3:c.456C>G, NM_003696.2:c.456C>G

Select item 14864998374.

rs1486499837 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:6796407 (GRCh38)
11:6817638 (GRCh37)
Canonical SPDI:: NC_000011.10:6796406:A:C
Gene:: OR6A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6796407A>C, NC_000011.9:g.6817638A>C

Select item 14864129165.

rs1486412916 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6795482 (GRCh38)
11:6816713 (GRCh37)
Canonical SPDI:: NC_000011.10:6795481:G:A
Gene:: OR6A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6795482G>A, NC_000011.9:g.6816713G>A, NM_003696.3:c.227C>T, NM_003696.2:c.227C>T, NP_003687.2:p.Thr76Ile

Select item 14863722056.

rs1486372205 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:6794861 (GRCh38)
11:6816092 (GRCh37)
Canonical SPDI:: NC_000011.10:6794860:T:C
Gene:: OR6A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6794861T>C, NC_000011.9:g.6816092T>C, NM_003696.3:c.848A>G, NM_003696.2:c.848A>G, NP_003687.2:p.Tyr283Cys

Select item 14861764297.

rs1486176429 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6797494 (GRCh38)
11:6818725 (GRCh37)
Canonical SPDI:: NC_000011.10:6797493:C:T
Gene:: OR6A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000162/3 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000029/4 (GnomAD)
T=0.00067/3 (Estonian)
HGVS:: NC_000011.10:g.6797494C>T, NC_000011.9:g.6818725C>T

Select item 14860384248.

rs1486038424 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:6794655 (GRCh38)
11:6815886 (GRCh37)
Canonical SPDI:: NC_000011.10:6794654:C:T
Gene:: OR6A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0.000084/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.6794655C>T, NC_000011.9:g.6815886C>T, NM_003696.3:c.*70G>A, NM_003696.2:c.*70G>A

Select item 14848907609.

rs1484890760 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:6795200 (GRCh38)
11:6816431 (GRCh37)
Canonical SPDI:: NC_000011.10:6795199:C:G
Gene:: OR6A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6795200C>G, NC_000011.9:g.6816431C>G, NM_003696.3:c.509G>C, NM_003696.2:c.509G>C, NP_003687.2:p.Gly170Ala

Select item 148455552410.

rs1484555524 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:6794258 (GRCh38)
11:6815489 (GRCh37)
Canonical SPDI:: NC_000011.10:6794257:T:C
Gene:: OR6A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.6794258T>C, NC_000011.9:g.6815489T>C, NM_003696.3:c.*467A>G

Select item 148441716611.

rs1484417166 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:6795385 (GRCh38)
11:6816616 (GRCh37)
Canonical SPDI:: NC_000011.10:6795384:A:G
Gene:: OR6A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.6795385A>G, NC_000011.9:g.6816616A>G, NM_003696.3:c.324T>C, NM_003696.2:c.324T>C

Select item 148310118312.

rs1483101183 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6794241 (GRCh38)
11:6815472 (GRCh37)
Canonical SPDI:: NC_000011.10:6794240:G:A
Gene:: OR6A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.6794241G>A, NC_000011.9:g.6815472G>A, NM_003696.3:c.*484C>T

Select item 148133908413.

rs1481339084 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:6796777 (GRCh38)
11:6818008 (GRCh37)
Canonical SPDI:: NC_000011.10:6796776:A:C
Gene:: OR6A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6796777A>C, NC_000011.9:g.6818008A>C

Select item 148016995114.

rs1480169951 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:6796613 (GRCh38)
11:6817844 (GRCh37)
Canonical SPDI:: NC_000011.10:6796612:A:G
Gene:: OR6A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.6796613A>G, NC_000011.9:g.6817844A>G

Select item 148013340515.

rs1480133405 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:6794144 (GRCh38)
11:6815375 (GRCh37)
Canonical SPDI:: NC_000011.10:6794143:A:T
Gene:: OR6A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000011.10:g.6794144A>T, NC_000011.9:g.6815375A>T, NM_003696.3:c.*581T>A

Select item 147971072216.

rs1479710722 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:6797311 (GRCh38)
11:6818542 (GRCh37)
Canonical SPDI:: NC_000011.10:6797310:T:C
Gene:: OR6A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6797311T>C, NC_000011.9:g.6818542T>C

Select item 147919006117.

rs1479190061 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:6796062 (GRCh38)
11:6817293 (GRCh37)
Canonical SPDI:: NC_000011.10:6796061:A:G
Gene:: OR6A2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6796062A>G, NC_000011.9:g.6817293A>G

Select item 147847800018.

rs1478478000 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6794749 (GRCh38)
11:6815980 (GRCh37)
Canonical SPDI:: NC_000011.10:6794748:G:A
Gene:: OR6A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.6794749G>A, NC_000011.9:g.6815980G>A, NM_003696.3:c.960C>T, NM_003696.2:c.960C>T

Select item 147790825719.

rs1477908257 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:6794644 (GRCh38)
11:6815875 (GRCh37)
Canonical SPDI:: NC_000011.10:6794643:G:A
Gene:: OR6A2 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.6794644G>A, NC_000011.9:g.6815875G>A, NM_003696.3:c.*81C>T, NM_003696.2:c.*81C>T

Select item 147623228020.

rs1476232280 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:6795141 (GRCh38)
11:6816372 (GRCh37)
Canonical SPDI:: NC_000011.10:6795140:G:C
Gene:: OR6A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.6795141G>C, NC_000011.9:g.6816372G>C, NM_003696.3:c.568C>G, NM_003696.2:c.568C>G, NP_003687.2:p.Leu190Val

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