SNP Links for Gene (Select 441208) - SNP

Links from Gene

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Select item 14915845341.

rs1491584534 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 7:32730129 (GRCh38)
7:32769742 (GRCh37)
Canonical SPDI:: NC_000007.14:32730129::T
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.32730129_32730130insT, NC_000007.13:g.32769741_32769742insT

Select item 14912256472.

rs1491225647 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>- [Show Flanks]
Chromosome:: 7:32730130 (GRCh38)
7:32769742 (GRCh37)
Canonical SPDI:: NC_000007.14:32730128:AAA:A
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.32730130_32730131del, NC_000007.13:g.32769742_32769743del

Select item 14907920913.

rs1490792091 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:32730268 (GRCh38)
7:32769880 (GRCh37)
Canonical SPDI:: NC_000007.14:32730267:C:T
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.32730268C>T, NC_000007.13:g.32769880C>T

Select item 14907763784.

rs1490776378 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:32729244 (GRCh38)
7:32768856 (GRCh37)
Canonical SPDI:: NC_000007.14:32729243:G:A
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.32729244G>A, NC_000007.13:g.32768856G>A, NR_003502.2:n.1295G>A, NM_001013723.1:c.*570G>A

Select item 14886590055.

rs1488659005 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:32726543 (GRCh38)
7:32766155 (GRCh37)
Canonical SPDI:: NC_000007.14:32726542:A:C
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.32726543A>C, NC_000007.13:g.32766155A>C

Select item 14870245576.

rs1487024557 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:32727007 (GRCh38)
7:32766619 (GRCh37)
Canonical SPDI:: NC_000007.14:32727006:A:C
Gene:: ZNRF2P1 (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_000007.14:g.32727007A>C, NC_000007.13:g.32766619A>C

Select item 14869114167.

rs1486911416 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:32729632 (GRCh38)
7:32769244 (GRCh37)
Canonical SPDI:: NC_000007.14:32729631:G:A
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.32729632G>A, NC_000007.13:g.32769244G>A, NR_003502.2:n.1683G>A, NM_001013723.1:c.*958G>A

Select item 14868814898.

rs1486881489 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:32728925 (GRCh38)
7:32768537 (GRCh37)
Canonical SPDI:: NC_000007.14:32728924:C:A
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000007.14:g.32728925C>A, NC_000007.13:g.32768537C>A, NR_003502.2:n.976C>A, NM_001013723.1:c.*278C>A

Select item 14868413329.

rs1486841332 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:32727081 (GRCh38)
7:32766693 (GRCh37)
Canonical SPDI:: NC_000007.14:32727080:A:C
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.32727081A>C, NC_000007.13:g.32766693A>C

Select item 148656435410.

rs1486564354 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:32726082 (GRCh38)
7:32765694 (GRCh37)
Canonical SPDI:: NC_000007.14:32726081:A:C
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.32726082A>C, NC_000007.13:g.32765694A>C

Select item 148538144111.

rs1485381441 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGCGGCGGCC [Show Flanks]
Chromosome:: 7:32728911 (GRCh38)
7:32768524 (GRCh37)
Canonical SPDI:: NC_000007.14:32728911:CGGCGGCGGCC:CGGCGGCGGCCGGCGGCGGCC
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: CGGCGGCGGCCGGCGGCGGCC=0./0 (ALFA)
CGGCGGCGGC=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.32728913_32728922dup, NC_000007.13:g.32768525_32768534dup, NR_003502.2:n.964_973dup, NM_001013723.1:c.*267A>G, NM_001013723.1:c.*267delinsGCGGCGGCCGG

Select item 148473960812.

rs1484739608 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:32728056 (GRCh38)
7:32767668 (GRCh37)
Canonical SPDI:: NC_000007.14:32728055:A:G
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_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_000007.14:g.32728056A>G, NC_000007.13:g.32767668A>G, NR_003502.2:n.107A>G

Select item 148445995713.

rs1484459957 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:32728622 (GRCh38)
7:32768234 (GRCh37)
Canonical SPDI:: NC_000007.14:32728621:C:T
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00006/1 (TOMMO)
HGVS:: NC_000007.14:g.32728622C>T, NC_000007.13:g.32768234C>T, NR_003502.2:n.673C>T, NM_001013723.1:c.383C>T

Select item 148377667614.

rs1483776676 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:32726223 (GRCh38)
7:32765835 (GRCh37)
Canonical SPDI:: NC_000007.14:32726222:G:A
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.32726223G>A, NC_000007.13:g.32765835G>A

Select item 148362920615.

rs1483629206 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:32729027 (GRCh38)
7:32768639 (GRCh37)
Canonical SPDI:: NC_000007.14:32729026:C:G,NC_000007.14:32729026:C:T
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.32729027C>G, NC_000007.14:g.32729027C>T, NC_000007.13:g.32768639C>G, NC_000007.13:g.32768639C>T, NR_003502.2:n.1078C>G, NR_003502.2:n.1078C>T, NM_001013723.1:c.*380C>G, NM_001013723.1:c.*380C>T

Select item 148341476916.

rs1483414769 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:32727391 (GRCh38)
7:32767003 (GRCh37)
Canonical SPDI:: NC_000007.14:32727390:G:A
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000023/6 (TOPMED)
A=0.000036/5 (GnomAD)
HGVS:: NC_000007.14:g.32727391G>A, NC_000007.13:g.32767003G>A

Select item 148330150217.

rs1483301502 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 7:32728832 (GRCh38)
7:32768444 (GRCh37)
Canonical SPDI:: NC_000007.14:32728831:T:C,NC_000007.14:32728831:T:G
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.32728832T>C, NC_000007.14:g.32728832T>G, NC_000007.13:g.32768444T>C, NC_000007.13:g.32768444T>G, NR_003502.2:n.883T>C, NR_003502.2:n.883T>G, NM_001013723.1:c.*185T>C, NM_001013723.1:c.*185T>G

Select item 148250003818.

rs1482500038 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:32729052 (GRCh38)
7:32768664 (GRCh37)
Canonical SPDI:: NC_000007.14:32729051:G:C
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000034/9 (TOPMED)
C=0.000035/1 (TOMMO)
HGVS:: NC_000007.14:g.32729052G>C, NC_000007.13:g.32768664G>C, NR_003502.2:n.1103G>C, NM_001013723.1:c.*405G>C

Select item 148177750319.

rs1481777503 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATTTA>- [Show Flanks]
Chromosome:: 7:32726586 (GRCh38)
7:32766198 (GRCh37)
Canonical SPDI:: NC_000007.14:32726584:AATTTA:A
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.00005/7 (GnomAD)
-=0.000057/15 (TOPMED)
HGVS:: NC_000007.14:g.32726586_32726590del, NC_000007.13:g.32766198_32766202del

Select item 148111942120.

rs1481119421 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:32728822 (GRCh38)
7:32768434 (GRCh37)
Canonical SPDI:: NC_000007.14:32728821:C:T
Gene:: ZNRF2P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.32728822C>T, NC_000007.13:g.32768434C>T, NR_003502.2:n.873C>T, NM_001013723.1:c.*175C>T

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