SNP Links for Gene (Select 2167) - SNP

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14909020331.

rs1490902033 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:81479405 (GRCh38)
8:82391640 (GRCh37)
Canonical SPDI:: NC_000008.11:81479404:G:T
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.81479405G>T, NC_000008.10:g.82391640G>T

Select item 14907266642.

rs1490726664 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:81484210 (GRCh38)
8:82396445 (GRCh37)
Canonical SPDI:: NC_000008.11:81484209:A:G
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,2KB_upstream_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.81484210A>G, NC_000008.10:g.82396445A>G

Select item 14907004963.

rs1490700496 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:81481748 (GRCh38)
8:82393983 (GRCh37)
Canonical SPDI:: NC_000008.11:81481747:G:A
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_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_000008.11:g.81481748G>A, NC_000008.10:g.82393983G>A

Select item 14905959844.

rs1490595984 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:81481811 (GRCh38)
8:82394046 (GRCh37)
Canonical SPDI:: NC_000008.11:81481810:A:G
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.81481811A>G, NC_000008.10:g.82394046A>G

Select item 14900804205.

rs1490080420 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:81480712 (GRCh38)
8:82392947 (GRCh37)
Canonical SPDI:: NC_000008.11:81480711:G:A
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000008.11:g.81480712G>A, NC_000008.10:g.82392947G>A

Select item 14898850886.

rs1489885088 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:81482733 (GRCh38)
8:82394968 (GRCh37)
Canonical SPDI:: NC_000008.11:81482732:A:G
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000036/5 (GnomAD)
HGVS:: NC_000008.11:g.81482733A>G, NC_000008.10:g.82394968A>G

Select item 14881710707.

rs1488171070 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:81479150 (GRCh38)
8:82391385 (GRCh37)
Canonical SPDI:: NC_000008.11:81479149:G:A
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.81479150G>A, NC_000008.10:g.82391385G>A

Select item 14874489898.

rs1487448989 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:81482394 (GRCh38)
8:82394629 (GRCh37)
Canonical SPDI:: NC_000008.11:81482393:C:T
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000008.11:g.81482394C>T, NC_000008.10:g.82394629C>T

Select item 14865303639.

rs1486530363 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 8:81478707 (GRCh38)
8:82390942 (GRCh37)
Canonical SPDI:: NC_000008.11:81478706:T:A
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000008.11:g.81478707T>A, NC_000008.10:g.82390942T>A, NM_001442.3:c.*158A>T, NM_001442.2:c.*158A>T

Select item 148549060510.

rs1485490605 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:81481237 (GRCh38)
8:82393472 (GRCh37)
Canonical SPDI:: NC_000008.11:81481236:T:G
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,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_000008.11:g.81481237T>G, NC_000008.10:g.82393472T>G

Select item 148522558611.

rs1485225586 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:81484332 (GRCh38)
8:82396567 (GRCh37)
Canonical SPDI:: NC_000008.11:81484331:G:A
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.81484332G>A, NC_000008.10:g.82396567G>A

Select item 148495478912.

rs1484954789 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:81484825 (GRCh38)
8:82397060 (GRCh37)
Canonical SPDI:: NC_000008.11:81484824:T:G
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.81484825T>G, NC_000008.10:g.82397060T>G

Select item 148340484113.

rs1483404841 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:81483711 (GRCh38)
8:82395946 (GRCh37)
Canonical SPDI:: NC_000008.11:81483710:G:A
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.81483711G>A, NC_000008.10:g.82395946G>A

Select item 148326637314.

rs1483266373 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:81483396 (GRCh38)
8:82395631 (GRCh37)
Canonical SPDI:: NC_000008.11:81483395:C:G
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0.000084/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.81483396C>G, NC_000008.10:g.82395631C>G

Select item 148303289015.

rs1483032890 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:81483370 (GRCh38)
8:82395605 (GRCh37)
Canonical SPDI:: NC_000008.11:81483369:A:C
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.81483370A>C, NC_000008.10:g.82395605A>C

Select item 148271055316.

rs1482710553 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 8:81479901 (GRCh38)
8:82392136 (GRCh37)
Canonical SPDI:: NC_000008.11:81479900:T:A,NC_000008.11:81479900:T:C
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.81479901T>A, NC_000008.11:g.81479901T>C, NC_000008.10:g.82392136T>A, NC_000008.10:g.82392136T>C

Select item 148229265017.

rs1482292650 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CATA [Show Flanks]
Chromosome:: 8:81479047 (GRCh38)
8:82391283 (GRCh37)
Canonical SPDI:: NC_000008.11:81479047:CATA:CATACATA
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CATACATA=0./0 (ALFA)
CATA=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.81479048_81479051dup, NC_000008.10:g.82391283_82391286dup

Select item 148184854218.

rs1481848542 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATTAAT>- [Show Flanks]
Chromosome:: 8:81482053 (GRCh38)
8:82394288 (GRCh37)
Canonical SPDI:: NC_000008.11:81482050:ATATTAAT:AT
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: AT=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.81482053_81482058del, NC_000008.10:g.82394288_82394293del

Select item 148159321919.

rs1481593219 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 8:81480619 (GRCh38)
8:82392854 (GRCh37)
Canonical SPDI:: NC_000008.11:81480618:G:A,NC_000008.11:81480618:G:T
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.81480619G>A, NC_000008.11:g.81480619G>T, NC_000008.10:g.82392854G>A, NC_000008.10:g.82392854G>T

Select item 148119044120.

rs1481190441 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:81481481 (GRCh38)
8:82393716 (GRCh37)
Canonical SPDI:: NC_000008.11:81481480:A:G
Gene:: FABP4 (Varview), LOC101927118 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000008.11:g.81481481A>G, NC_000008.10:g.82393716A>G

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 1000

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity