SNP Links for Gene (Select 441025) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 20 of 2723

<< First< Prev

Page of 137

Next >Last >>

Select item 14907096771.

rs1490709677 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:75354932 (GRCh38)
4:76280142 (GRCh37)
Canonical SPDI:: NC_000004.12:75354931:A:G
Gene:: LINC02483 (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_000004.12:g.75354932A>G, NC_000004.11:g.76280142A>G

Select item 14903311592.

rs1490331159 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:75354107 (GRCh38)
4:76279317 (GRCh37)
Canonical SPDI:: NC_000004.12:75354106:A:C
Gene:: LINC02483 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000142/2 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.75354107A>C, NC_000004.11:g.76279317A>C, NR_033964.1:n.32A>C

Select item 14903290643.

rs1490329064 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:75352442 (GRCh38)
4:76277652 (GRCh37)
Canonical SPDI:: NC_000004.12:75352441:G:A
Gene:: LINC02483 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
HGVS:: NC_000004.12:g.75352442G>A, NC_000004.11:g.76277652G>A

Select item 14902801004.

rs1490280100 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:75352153 (GRCh38)
4:76277363 (GRCh37)
Canonical SPDI:: NC_000004.12:75352152:C:T
Gene:: LINC02483 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.75352153C>T, NC_000004.11:g.76277363C>T

Select item 14902554465.

rs1490255446 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:75356103 (GRCh38)
4:76281313 (GRCh37)
Canonical SPDI:: NC_000004.12:75356102:A:C
Gene:: LINC02483 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.75356103A>C, NC_000004.11:g.76281313A>C

Select item 14901705306.

rs1490170530 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 4:75362683 (GRCh38)
4:76287893 (GRCh37)
Canonical SPDI:: NC_000004.12:75362682:G:
Gene:: LINC02483 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000042/11 (TOPMED)
HGVS:: NC_000004.12:g.75362683del, NC_000004.11:g.76287893del

Select item 14898414867.

rs1489841486 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:75353145 (GRCh38)
4:76278355 (GRCh37)
Canonical SPDI:: NC_000004.12:75353144:A:G
Gene:: LINC02483 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000004.12:g.75353145A>G, NC_000004.11:g.76278355A>G

Select item 14897587028.

rs1489758702 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:75354150 (GRCh38)
4:76279360 (GRCh37)
Canonical SPDI:: NC_000004.12:75354149:A:C
Gene:: LINC02483 (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_000004.12:g.75354150A>C, NC_000004.11:g.76279360A>C

Select item 14893730399.

rs1489373039 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:75353841 (GRCh38)
4:76279051 (GRCh37)
Canonical SPDI:: NC_000004.12:75353840:G:C
Gene:: LINC02483 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000004.12:g.75353841G>C, NC_000004.11:g.76279051G>C

Select item 148920032810.

rs1489200328 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:75359360 (GRCh38)
4:76284570 (GRCh37)
Canonical SPDI:: NC_000004.12:75359359:T:C
Gene:: LINC02483 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000094/1 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000004.12:g.75359360T>C, NC_000004.11:g.76284570T>C

Select item 148839052111.

rs1488390521 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:75354153 (GRCh38)
4:76279363 (GRCh37)
Canonical SPDI:: NC_000004.12:75354152:T:A
Gene:: LINC02483 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000084/1 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000004.12:g.75354153T>A, NC_000004.11:g.76279363T>A

Select item 148806593712.

rs1488065937 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:75361803 (GRCh38)
4:76287013 (GRCh37)
Canonical SPDI:: NC_000004.12:75361802:G:A
Gene:: LINC02483 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.75361803G>A, NC_000004.11:g.76287013G>A, NR_033964.1:n.380G>A

Select item 148795852513.

rs1487958525 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:75353832 (GRCh38)
4:76279042 (GRCh37)
Canonical SPDI:: NC_000004.12:75353831:C:A
Gene:: LINC02483 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.75353832C>A, NC_000004.11:g.76279042C>A

Select item 148776097014.

rs1487760970 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:75354082 (GRCh38)
4:76279292 (GRCh37)
Canonical SPDI:: NC_000004.12:75354081:T:A
Gene:: LINC02483 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000004.12:g.75354082T>A, NC_000004.11:g.76279292T>A, NR_033964.1:n.7T>A

Select item 148724680115.

rs1487246801 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:75357548 (GRCh38)
4:76282758 (GRCh37)
Canonical SPDI:: NC_000004.12:75357547:C:G
Gene:: LINC02483 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.75357548C>G, NC_000004.11:g.76282758C>G

Select item 148723069016.

rs1487230690 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:75361872 (GRCh38)
4:76287082 (GRCh37)
Canonical SPDI:: NC_000004.12:75361871:A:G
Gene:: LINC02483 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.75361872A>G, NC_000004.11:g.76287082A>G, NR_033964.1:n.449A>G

Select item 148721947217.

rs1487219472 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:75360916 (GRCh38)
4:76286126 (GRCh37)
Canonical SPDI:: NC_000004.12:75360915:A:G
Gene:: LINC02483 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000004.12:g.75360916A>G, NC_000004.11:g.76286126A>G

Select item 148721565818.

rs1487215658 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:75355502 (GRCh38)
4:76280712 (GRCh37)
Canonical SPDI:: NC_000004.12:75355501:G:C
Gene:: LINC02483 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000043/6 (GnomAD)
C=0.000049/13 (TOPMED)
HGVS:: NC_000004.12:g.75355502G>C, NC_000004.11:g.76280712G>C

Select item 148698449719.

rs1486984497 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:75362757 (GRCh38)
4:76287967 (GRCh37)
Canonical SPDI:: NC_000004.12:75362756:C:G
Gene:: LINC02483 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.75362757C>G, NC_000004.11:g.76287967C>G

Select item 148679485020.

rs1486794850 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:75357918 (GRCh38)
4:76283128 (GRCh37)
Canonical SPDI:: NC_000004.12:75357917:T:A
Gene:: LINC02483 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.75357918T>A, NC_000004.11:g.76283128T>A

<< First< Prev

Page of 137

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Gene (Select 441025) (2723)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: