SNP Links for Gene (Select 392390) - SNP

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Select item 14883169621.

rs1488316962 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:122750540 (GRCh38)
9:125512819 (GRCh37)
Canonical SPDI:: NC_000009.12:122750539:T:C
Gene:: OR1L6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.122750540T>C, NC_000009.11:g.125512819T>C, NG_034003.1:g.5693T>C, NM_001004453.2:c.693T>C, NM_001004453.3:c.693T>C

Select item 14881442832.

rs1488144283 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:122750528 (GRCh38)
9:125512807 (GRCh37)
Canonical SPDI:: NC_000009.12:122750527:C:T
Gene:: OR1L6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.122750528C>T, NC_000009.11:g.125512807C>T, NG_034003.1:g.5681C>T, NM_001004453.2:c.681C>T, NM_001004453.3:c.681C>T

Select item 14859606063.

rs1485960606 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:122750042 (GRCh38)
9:125512321 (GRCh37)
Canonical SPDI:: NC_000009.12:122750041:C:A
Gene:: OR1L6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122750042C>A, NC_000009.11:g.125512321C>A, NG_034003.1:g.5195C>A, NM_001004453.2:c.195C>A, NM_001004453.3:c.195C>A, NP_001004453.2:p.Ser65Arg

Select item 14857539854.

rs1485753985 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:122749576 (GRCh38)
9:125511855 (GRCh37)
Canonical SPDI:: NC_000009.12:122749575:C:T
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000029/4 (GnomAD)
T=0.000038/10 (TOPMED)
HGVS:: NC_000009.12:g.122749576C>T, NC_000009.11:g.125511855C>T, NG_034003.1:g.4729C>T

Select item 14853942465.

rs1485394246 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:122750149 (GRCh38)
9:125512428 (GRCh37)
Canonical SPDI:: NC_000009.12:122750148:A:C
Gene:: OR1L6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000009.12:g.122750149A>C, NC_000009.11:g.125512428A>C, NG_034003.1:g.5302A>C, NM_001004453.2:c.302A>C, NM_001004453.3:c.302A>C, NP_001004453.2:p.Gln101Pro

Select item 14843486826.

rs1484348682 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:122748741 (GRCh38)
9:125511020 (GRCh37)
Canonical SPDI:: NC_000009.12:122748740:A:G
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.122748741A>G, NC_000009.11:g.125511020A>G, NG_034003.1:g.3894A>G

Select item 14843388807.

rs1484338880 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:122748363 (GRCh38)
9:125510642 (GRCh37)
Canonical SPDI:: NC_000009.12:122748362:T:G
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000036/5 (GnomAD)
HGVS:: NC_000009.12:g.122748363T>G, NC_000009.11:g.125510642T>G, NG_034003.1:g.3516T>G

Select item 14835168428.

rs1483516842 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:122749148 (GRCh38)
9:125511427 (GRCh37)
Canonical SPDI:: NC_000009.12:122749147:G:C
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000009.12:g.122749148G>C, NC_000009.11:g.125511427G>C, NG_034003.1:g.4301G>C

Select item 14827184699.

rs1482718469 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:122748300 (GRCh38)
9:125510579 (GRCh37)
Canonical SPDI:: NC_000009.12:122748299:G:A
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.122748300G>A, NC_000009.11:g.125510579G>A, NG_034003.1:g.3453G>A

Select item 148257080710.

rs1482570807 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:122750313 (GRCh38)
9:125512592 (GRCh37)
Canonical SPDI:: NC_000009.12:122750312:C:T
Gene:: OR1L6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122750313C>T, NC_000009.11:g.125512592C>T, NG_034003.1:g.5466C>T, NM_001004453.2:c.466C>T, NM_001004453.3:c.466C>T, NP_001004453.2:p.His156Tyr

Select item 148246690911.

rs1482466909 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:122750318 (GRCh38)
9:125512597 (GRCh37)
Canonical SPDI:: NC_000009.12:122750317:C:A,NC_000009.12:122750317:C:T
Gene:: OR1L6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.122750318C>A, NC_000009.12:g.122750318C>T, NC_000009.11:g.125512597C>A, NC_000009.11:g.125512597C>T, NG_034003.1:g.5471C>A, NG_034003.1:g.5471C>T, NM_001004453.2:c.471C>A, NM_001004453.2:c.471C>T, NM_001004453.3:c.471C>A, NM_001004453.3:c.471C>T

Select item 147934292112.

rs1479342921 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 9:122749757 (GRCh38)
9:125512036 (GRCh37)
Canonical SPDI:: NC_000009.12:122749756:G:C,NC_000009.12:122749756:G:T
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
T=0.000071/2 (TOMMO)
HGVS:: NC_000009.12:g.122749757G>C, NC_000009.12:g.122749757G>T, NC_000009.11:g.125512036G>C, NC_000009.11:g.125512036G>T, NG_034003.1:g.4910G>C, NG_034003.1:g.4910G>T

Select item 147793491513.

rs1477934915 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:122750708 (GRCh38)
9:125512987 (GRCh37)
Canonical SPDI:: NC_000009.12:122750707:C:T
Gene:: OR1L6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.122750708C>T, NC_000009.11:g.125512987C>T, NG_034003.1:g.5861C>T, NM_001004453.2:c.861C>T, NM_001004453.3:c.861C>T

Select item 147688826914.

rs1476888269 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:122748416 (GRCh38)
9:125510695 (GRCh37)
Canonical SPDI:: NC_000009.12:122748415:G:C
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.122748416G>C, NC_000009.11:g.125510695G>C, NG_034003.1:g.3569G>C

Select item 147613143815.

rs1476131438 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:122751117 (GRCh38)
9:125513396 (GRCh37)
Canonical SPDI:: NC_000009.12:122751116:T:C
Gene:: OR1L6 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.122751117T>C, NC_000009.11:g.125513396T>C, NG_034003.1:g.6270T>C

Select item 147503076716.

rs1475030767 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:122750992 (GRCh38)
9:125513271 (GRCh37)
Canonical SPDI:: NC_000009.12:122750991:G:C
Gene:: OR1L6 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000224/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000009.12:g.122750992G>C, NC_000009.11:g.125513271G>C, NG_034003.1:g.6145G>C

Select item 147489010017.

rs1474890100 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:122749206 (GRCh38)
9:125511485 (GRCh37)
Canonical SPDI:: NC_000009.12:122749205:T:C
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.122749206T>C, NC_000009.11:g.125511485T>C, NG_034003.1:g.4359T>C

Select item 147410579818.

rs1474105798 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:122749345 (GRCh38)
9:125511624 (GRCh37)
Canonical SPDI:: NC_000009.12:122749344:A:G
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.122749345A>G, NC_000009.11:g.125511624A>G, NG_034003.1:g.4498A>G

Select item 147401478519.

rs1474014785 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:122748249 (GRCh38)
9:125510528 (GRCh37)
Canonical SPDI:: NC_000009.12:122748248:T:C
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.122748249T>C, NC_000009.11:g.125510528T>C, NG_034003.1:g.3402T>C

Select item 147359795920.

rs1473597959 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:122748111 (GRCh38)
9:125510390 (GRCh37)
Canonical SPDI:: NC_000009.12:122748110:C:T
Gene:: OR1L6 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.122748111C>T, NC_000009.11:g.125510390C>T, NG_034003.1:g.3264C>T

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