SNP Links for Gene (Select 282616) - SNP

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14914170001.

rs1491417000 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CC [Show Flanks]
Chromosome:: 19:39269318 (GRCh38)
19:39759959 (GRCh37)
Canonical SPDI:: NC_000019.10:39269318:C:CCC
Gene:: IFNL2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCC=0./0 (ALFA)
CC=0.000007/1 (GnomAD)
CC=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.39269319_39269320insCC, NC_000019.9:g.39759959_39759960insCC, NW_025791808.1:g.49701_49702insCC

Select item 14912929252.

rs1491292925 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCT>-,CT,CTCTCT [Show Flanks]
Chromosome:: 19:39269325 (GRCh38)
19:39759965 (GRCh37)
Canonical SPDI:: NC_000019.10:39269317:TCTCTCTCTCT:TCTCTCT,NC_000019.10:39269317:TCTCTCTCTCT:TCTCTCTCT,NC_000019.10:39269317:TCTCTCTCTCT:TCTCTCTCTCTCT
Gene:: IFNL2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCTCTCT=0./0 (ALFA)
HGVS:: NC_000019.10:g.39269319CT[3], NC_000019.10:g.39269319CT[4], NC_000019.10:g.39269319CT[6], NC_000019.9:g.39759959CT[3], NC_000019.9:g.39759959CT[4], NC_000019.9:g.39759959CT[6], NW_025791808.1:g.49701CT[3], NW_025791808.1:g.49701CT[4], NW_025791808.1:g.49701CT[6]

Select item 14911562023.

rs1491156202 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TACA,TACACA,TACACACA,TATACA,TATACACA,TATATACA,TATATACACA,TATATATACA,TATATATACACA,TATATATACACACA,TATATATATACA,TATATATATACACA,TATATATATACACACA,TATATATATATACA,TATATATATATACACA,TATATATATATACACACA,TATATATATATATACA,TATATATATATATACACA,TATATATATATATATACA,TATATATATATATATACACA,TATATATATATATATATACA,TATATATATATATATATACACA,TATATATATATATATATATACA,TATATATATATATATATATACACA,TATATATATATATATATATATACA,TATATATATATATATATATATACATACA,TATATATATATATATATATATATACA,TATATATATATATATATATATATACACA,TATATATATATATATATATATATATACA,TATATATATATATATATATATATATATACA,TATATATATATATATATATATATATATATACA,TATATATATATATATATATATATATATATATACA,TATATATATATATATATATGTATATACA,TATATATATATATATATGTATATACA,TATATATATATATATGTATATACA,TATATATATATATGTATATACA,TATATATATATGTATATACA [Show Flanks]
Chromosome:: 19:39267360 (GRCh38)
19:39758001 (GRCh37)
Canonical SPDI:: NC_000019.10:39267360:A:ATACA,NC_000019.10:39267360:A:ATACACA,NC_000019.10:39267360:A:ATACACACA,NC_000019.10:39267360:A:ATATACA,NC_000019.10:39267360:A:ATATACACA,NC_000019.10:39267360:A:ATATATACA,NC_000019.10:39267360:A:ATATATACACA,NC_000019.10:39267360:A:ATATATATACA,NC_000019.10:39267360:A:ATATATATACACA,NC_000019.10:39267360:A:ATATATATACACACA,NC_000019.10:39267360:A:ATATATATATACA,NC_000019.10:39267360:A:ATATATATATACACA,NC_000019.10:39267360:A:ATATATATATACACACA,NC_000019.10:39267360:A:ATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATACACA,NC_000019.10:39267360:A:ATATATATATATACACACA,NC_000019.10:39267360:A:ATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATACACA,NC_000019.10:39267360:A:ATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATACACA,NC_000019.10:39267360:A:ATATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATATACACA,NC_000019.10:39267360:A:ATATATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATATATACACA,NC_000019.10:39267360:A:ATATATATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATATATATACATACA,NC_000019.10:39267360:A:ATATATATATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATATATATATACACA,NC_000019.10:39267360:A:ATATATATATATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATATATATATATATATATACA,NC_000019.10:39267360:A:ATATATATATATATATATATGTATATACA,NC_000019.10:39267360:A:ATATATATATATATATATGTATATACA,NC_000019.10:39267360:A:ATATATATATATATATGTATATACA,NC_000019.10:39267360:A:ATATATATATATATGTATATACA,NC_000019.10:39267360:A:ATATATATATATGTATATACA
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATACACA=0./0 (ALFA)
HGVS:: NC_000019.10:g.39267361_39267362insTACA, NC_000019.10:g.39267361_39267362insTACACA, NC_000019.10:g.39267361_39267362insTACACACA, NC_000019.10:g.39267361AT[2]ACA[1], NC_000019.10:g.39267361AT[2]AC[2]A[1], NC_000019.10:g.39267361AT[3]ACA[1], NC_000019.10:g.39267361AT[3]AC[2]A[1], NC_000019.10:g.39267361AT[4]ACA[1], NC_000019.10:g.39267361AT[4]AC[2]A[1], NC_000019.10:g.39267361AT[4]AC[3]A[1], NC_000019.10:g.39267361AT[5]ACA[1], NC_000019.10:g.39267361AT[5]AC[2]A[1], NC_000019.10:g.39267361AT[5]AC[3]A[1], NC_000019.10:g.39267361AT[6]ACA[1], NC_000019.10:g.39267361AT[6]AC[2]A[1], NC_000019.10:g.39267361AT[6]AC[3]A[1], NC_000019.10:g.39267361AT[7]ACA[1], NC_000019.10:g.39267361AT[7]AC[2]A[1], NC_000019.10:g.39267361AT[8]ACA[1], NC_000019.10:g.39267361AT[8]AC[2]A[1], NC_000019.10:g.39267361AT[9]ACA[1], NC_000019.10:g.39267361AT[9]AC[2]A[1], NC_000019.10:g.39267361AT[10]ACA[1], NC_000019.10:g.39267361AT[10]AC[2]A[1], NC_000019.10:g.39267361AT[11]ACA[1], NC_000019.10:g.39267361AT[11]ACATACA[1], NC_000019.10:g.39267361AT[12]ACA[1], NC_000019.10:g.39267361AT[12]AC[2]A[1], NC_000019.10:g.39267361AT[13]ACA[1], NC_000019.10:g.39267361AT[14]ACA[1], NC_000019.10:g.39267361AT[15]ACA[1], NC_000019.10:g.39267361AT[16]ACA[1], NC_000019.10:g.39267361AT[10]GTATATACA[1], NC_000019.10:g.39267361AT[9]GTATATACA[1], NC_000019.10:g.39267361AT[8]GTATATACA[1], NC_000019.10:g.39267361AT[7]GTATATACA[1], NC_000019.10:g.39267361AT[6]GTATATACA[1], NC_000019.9:g.39758001_39758002insTACA, NC_000019.9:g.39758001_39758002insTACACA, NC_000019.9:g.39758001_39758002insTACACACA, NC_000019.9:g.39758001AT[2]ACA[1], NC_000019.9:g.39758001AT[2]AC[2]A[1], NC_000019.9:g.39758001AT[3]ACA[1], NC_000019.9:g.39758001AT[3]AC[2]A[1], NC_000019.9:g.39758001AT[4]ACA[1], NC_000019.9:g.39758001AT[4]AC[2]A[1], NC_000019.9:g.39758001AT[4]AC[3]A[1], NC_000019.9:g.39758001AT[5]ACA[1], NC_000019.9:g.39758001AT[5]AC[2]A[1], NC_000019.9:g.39758001AT[5]AC[3]A[1], NC_000019.9:g.39758001AT[6]ACA[1], NC_000019.9:g.39758001AT[6]AC[2]A[1], NC_000019.9:g.39758001AT[6]AC[3]A[1], NC_000019.9:g.39758001AT[7]ACA[1], NC_000019.9:g.39758001AT[7]AC[2]A[1], NC_000019.9:g.39758001AT[8]ACA[1], NC_000019.9:g.39758001AT[8]AC[2]A[1], NC_000019.9:g.39758001AT[9]ACA[1], NC_000019.9:g.39758001AT[9]AC[2]A[1], NC_000019.9:g.39758001AT[10]ACA[1], NC_000019.9:g.39758001AT[10]AC[2]A[1], NC_000019.9:g.39758001AT[11]ACA[1], NC_000019.9:g.39758001AT[11]ACATACA[1], NC_000019.9:g.39758001AT[12]ACA[1], NC_000019.9:g.39758001AT[12]AC[2]A[1], NC_000019.9:g.39758001AT[13]ACA[1], NC_000019.9:g.39758001AT[14]ACA[1], NC_000019.9:g.39758001AT[15]ACA[1], NC_000019.9:g.39758001AT[16]ACA[1], NC_000019.9:g.39758001AT[10]GTATATACA[1], NC_000019.9:g.39758001AT[9]GTATATACA[1], NC_000019.9:g.39758001AT[8]GTATATACA[1], NC_000019.9:g.39758001AT[7]GTATATACA[1], NC_000019.9:g.39758001AT[6]GTATATACA[1], NW_025791808.1:g.47743_47744insTACA, NW_025791808.1:g.47743_47744insTACACA, NW_025791808.1:g.47743_47744insTACACACA, NW_025791808.1:g.47743AT[2]ACA[1], NW_025791808.1:g.47743AT[2]AC[2]A[1], NW_025791808.1:g.47743AT[3]ACA[1], NW_025791808.1:g.47743AT[3]AC[2]A[1], NW_025791808.1:g.47743AT[4]ACA[1], NW_025791808.1:g.47743AT[4]AC[2]A[1], NW_025791808.1:g.47743AT[4]AC[3]A[1], NW_025791808.1:g.47743AT[5]ACA[1], NW_025791808.1:g.47743AT[5]AC[2]A[1], NW_025791808.1:g.47743AT[5]AC[3]A[1], NW_025791808.1:g.47743AT[6]ACA[1], NW_025791808.1:g.47743AT[6]AC[2]A[1], NW_025791808.1:g.47743AT[6]AC[3]A[1], NW_025791808.1:g.47743AT[7]ACA[1], NW_025791808.1:g.47743AT[7]AC[2]A[1], NW_025791808.1:g.47743AT[8]ACA[1], NW_025791808.1:g.47743AT[8]AC[2]A[1], NW_025791808.1:g.47743AT[9]ACA[1], NW_025791808.1:g.47743AT[9]AC[2]A[1], NW_025791808.1:g.47743AT[10]ACA[1], NW_025791808.1:g.47743AT[10]AC[2]A[1], NW_025791808.1:g.47743AT[11]ACA[1], NW_025791808.1:g.47743AT[11]ACATACA[1], NW_025791808.1:g.47743AT[12]ACA[1], NW_025791808.1:g.47743AT[12]AC[2]A[1], NW_025791808.1:g.47743AT[13]ACA[1], NW_025791808.1:g.47743AT[14]ACA[1], NW_025791808.1:g.47743AT[15]ACA[1], NW_025791808.1:g.47743AT[16]ACA[1], NW_025791808.1:g.47743AT[10]GTATATACA[1], NW_025791808.1:g.47743AT[9]GTATATACA[1], NW_025791808.1:g.47743AT[8]GTATATACA[1], NW_025791808.1:g.47743AT[7]GTATATACA[1], NW_025791808.1:g.47743AT[6]GTATATACA[1]

Select item 14908181194.

rs1490818119 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:39268539 (GRCh38)
19:39759179 (GRCh37)
Canonical SPDI:: NC_000019.10:39268538:T:A
Gene:: IFNL2 (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.39268539T>A, NC_000019.9:g.39759179T>A, NW_025791808.1:g.48921T>A, NM_172138.2:c.-30T>A, NM_172138.1:c.-30T>A

Select item 14895652765.

rs1489565276 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39267104 (GRCh38)
19:39757744 (GRCh37)
Canonical SPDI:: NC_000019.10:39267103:C:T
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000019.10:g.39267104C>T, NC_000019.9:g.39757744C>T, NW_025791808.1:g.47486C>T

Select item 14888959726.

rs1488895972 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:39270323 (GRCh38)
19:39760963 (GRCh37)
Canonical SPDI:: NC_000019.10:39270322:G:C
Gene:: IFNL2 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000142/2 (ALFA)
C=0.000019/5 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000019.10:g.39270323G>C, NC_000019.9:g.39760963G>C, NW_025791808.1:g.50705G>C

Select item 14872683707.

rs1487268370 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCTCTCTATATATAT>- [Show Flanks]
Chromosome:: 19:39267329 (GRCh38)
19:39757969 (GRCh37)
Canonical SPDI:: NC_000019.10:39267327:TCTCTCTCTATATATAT:T
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000337/4 (ALFA)
-=0.000711/75 (GnomAD)
HGVS:: NC_000019.10:g.39267329_39267344del, NC_000019.9:g.39757969_39757984del, NW_025791808.1:g.47711_47726del

Select item 14870840568.

rs1487084056 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:39268070 (GRCh38)
19:39758710 (GRCh37)
Canonical SPDI:: NC_000019.10:39268069:C:A
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.39268070C>A, NC_000019.9:g.39758710C>A, NW_025791808.1:g.48452C>A

Select item 14865178579.

rs1486517857 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:39267371 (GRCh38)
19:39758011 (GRCh37)
Canonical SPDI:: NC_000019.10:39267370:A:G
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000122/2 (ALFA)
G=0.000022/3 (GnomAD)
HGVS:: NC_000019.10:g.39267371A>G, NC_000019.9:g.39758011A>G, NW_025791808.1:g.47753A>G

Select item 148499196510.

rs1484991965 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 19:39267326 (GRCh38)
19:39757966 (GRCh37)
Canonical SPDI:: NC_000019.10:39267325:T:A,NC_000019.10:39267325:T:C
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000019.10:g.39267326T>A, NC_000019.10:g.39267326T>C, NC_000019.9:g.39757966T>A, NC_000019.9:g.39757966T>C, NW_025791808.1:g.47708T>A, NW_025791808.1:g.47708T>C

Select item 148488625311.

rs1484886253 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 19:39266549 (GRCh38)
19:39757190 (GRCh37)
Canonical SPDI:: NC_000019.10:39266549:TT:TTT
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTT=0./0 (ALFA)
HGVS:: NC_000019.10:g.39266551dup, NC_000019.9:g.39757191dup, NW_025791808.1:g.46933dup

Select item 148418735412.

rs1484187354 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39268870 (GRCh38)
19:39759510 (GRCh37)
Canonical SPDI:: NC_000019.10:39268869:C:T
Gene:: IFNL2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.39268870C>T, NC_000019.9:g.39759510C>T, NW_025791808.1:g.49252C>T

Select item 148386214713.

rs1483862147 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 19:39268583 (GRCh38)
19:39759223 (GRCh37)
Canonical SPDI:: NC_000019.10:39268582:G:T
Gene:: IFNL2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.39268583G>T, NC_000019.9:g.39759223G>T, NW_025791808.1:g.48965G>T

Select item 148280962414.

rs1482809624 has merged into rs113805808 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATAT>-,AT,ATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATACATATATATATATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT,ATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATAT [Show Flanks]
Chromosome:: 19:39267996 (GRCh38)
19:39758636 (GRCh37)
Canonical SPDI:: NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATACATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000019.10:39267983:ATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATATATATAT=0./0 (ALFA)
AT=0.25679/1286 (1000Genomes)
HGVS:: NC_000019.10:g.39267984AT[6], NC_000019.10:g.39267984AT[7], NC_000019.10:g.39267984AT[8], NC_000019.10:g.39267984AT[10], NC_000019.10:g.39267984AT[11], NC_000019.10:g.39267984AT[12], NC_000019.10:g.39267984_39268001AT[12]ACATATATATATATATATATATAT[1], NC_000019.10:g.39267984AT[13], NC_000019.10:g.39267984AT[14], NC_000019.10:g.39267984AT[15], NC_000019.10:g.39267984AT[16], NC_000019.10:g.39267984AT[17], NC_000019.10:g.39267984AT[18], NC_000019.10:g.39267984AT[19], NC_000019.10:g.39267984AT[20], NC_000019.10:g.39267984AT[21], NC_000019.10:g.39267984AT[22], NC_000019.10:g.39267984AT[23], NC_000019.10:g.39267984AT[24], NC_000019.10:g.39267984AT[25], NC_000019.10:g.39267984AT[26], NC_000019.10:g.39267984AT[27], NC_000019.10:g.39267984AT[29], NC_000019.10:g.39267984AT[30], NC_000019.10:g.39267984AT[32], NC_000019.9:g.39758624AT[6], NC_000019.9:g.39758624AT[7], NC_000019.9:g.39758624AT[8], NC_000019.9:g.39758624AT[10], NC_000019.9:g.39758624AT[11], NC_000019.9:g.39758624AT[12], NC_000019.9:g.39758624_39758641AT[12]ACATATATATATATATATATATAT[1], NC_000019.9:g.39758624AT[13], NC_000019.9:g.39758624AT[14], NC_000019.9:g.39758624AT[15], NC_000019.9:g.39758624AT[16], NC_000019.9:g.39758624AT[17], NC_000019.9:g.39758624AT[18], NC_000019.9:g.39758624AT[19], NC_000019.9:g.39758624AT[20], NC_000019.9:g.39758624AT[21], NC_000019.9:g.39758624AT[22], NC_000019.9:g.39758624AT[23], NC_000019.9:g.39758624AT[24], NC_000019.9:g.39758624AT[25], NC_000019.9:g.39758624AT[26], NC_000019.9:g.39758624AT[27], NC_000019.9:g.39758624AT[29], NC_000019.9:g.39758624AT[30], NC_000019.9:g.39758624AT[32], NW_025791808.1:g.48366AT[6], NW_025791808.1:g.48366AT[7], NW_025791808.1:g.48366AT[8], NW_025791808.1:g.48366AT[10], NW_025791808.1:g.48366AT[11], NW_025791808.1:g.48366AT[12], NW_025791808.1:g.48366_48383AT[12]ACATATATATATATATATATATAT[1], NW_025791808.1:g.48366AT[13], NW_025791808.1:g.48366AT[14], NW_025791808.1:g.48366AT[15], NW_025791808.1:g.48366AT[16], NW_025791808.1:g.48366AT[17], NW_025791808.1:g.48366AT[18], NW_025791808.1:g.48366AT[19], NW_025791808.1:g.48366AT[20], NW_025791808.1:g.48366AT[21], NW_025791808.1:g.48366AT[22], NW_025791808.1:g.48366AT[23], NW_025791808.1:g.48366AT[24], NW_025791808.1:g.48366AT[25], NW_025791808.1:g.48366AT[26], NW_025791808.1:g.48366AT[27], NW_025791808.1:g.48366AT[29], NW_025791808.1:g.48366AT[30], NW_025791808.1:g.48366AT[32]

Select item 148265474515.

rs1482654745 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:39270004 (GRCh38)
19:39760644 (GRCh37)
Canonical SPDI:: NC_000019.10:39270003:G:A
Gene:: IFNL2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000019.10:g.39270004G>A, NC_000019.9:g.39760644G>A, NW_025791808.1:g.50386G>A, NM_172138.2:c.594G>A, NM_172138.1:c.594G>A

Select item 148143336416.

rs1481433364 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39267658 (GRCh38)
19:39758298 (GRCh37)
Canonical SPDI:: NC_000019.10:39267657:C:T
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.39267658C>T, NC_000019.9:g.39758298C>T, NW_025791808.1:g.48040C>T

Select item 148065408117.

rs1480654081 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 19:39269302 (GRCh38)
19:39759942 (GRCh37)
Canonical SPDI:: NC_000019.10:39269301:G:A,NC_000019.10:39269301:G:C,NC_000019.10:39269301:G:T
Gene:: IFNL2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000035/1 (TOMMO)
T=0.000468/3 (1000Genomes)
HGVS:: NC_000019.10:g.39269302G>A, NC_000019.10:g.39269302G>C, NC_000019.10:g.39269302G>T, NC_000019.9:g.39759942G>A, NC_000019.9:g.39759942G>C, NC_000019.9:g.39759942G>T, NW_025791808.1:g.49684G>A, NW_025791808.1:g.49684G>C, NW_025791808.1:g.49684G>T

Select item 148041022418.

rs1480410224 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39269045 (GRCh38)
19:39759685 (GRCh37)
Canonical SPDI:: NC_000019.10:39269044:C:T
Gene:: IFNL2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.39269045C>T, NC_000019.9:g.39759685C>T, NW_025791808.1:g.49427C>T

Select item 148037072419.

rs1480370724 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:39268190 (GRCh38)
19:39758830 (GRCh37)
Canonical SPDI:: NC_000019.10:39268189:T:C
Gene:: IFNL2 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.39268190T>C, NC_000019.9:g.39758830T>C, NW_025791808.1:g.48572T>C

Select item 148029610820.

rs1480296108 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:39268617 (GRCh38)
19:39759257 (GRCh37)
Canonical SPDI:: NC_000019.10:39268616:C:T
Gene:: IFNL2 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.39268617C>T, NC_000019.9:g.39759257C>T, NW_025791808.1:g.48999C>T

<< First< Prev

Page of 50

Next >Last >>

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