SNP Links for Gene (Select 340544) - SNP

Links from Gene

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Select item 14902869741.

rs1490286974 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:103691679 (GRCh38)
X:102946607 (GRCh37)
Canonical SPDI:: NC_000023.11:103691678:A:G
Gene:: MORF4L2-AS1 (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=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103691679A>G, NC_000023.10:g.102946607A>G, NR_038978.1:n.1993A>G

Select item 14888045422.

rs1488804542 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:103690042 (GRCh38)
X:102944970 (GRCh37)
Canonical SPDI:: NC_000023.11:103690041:T:C
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103690042T>C, NC_000023.10:g.102944970T>C

Select item 14887747293.

rs1488774729 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:103690639 (GRCh38)
X:102945567 (GRCh37)
Canonical SPDI:: NC_000023.11:103690638:C:T
Gene:: MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103690639C>T, NC_000023.10:g.102945567C>T

Select item 14887129304.

rs1488712930 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:103691883 (GRCh38)
X:102946811 (GRCh37)
Canonical SPDI:: NC_000023.11:103691882:C:G
Gene:: MORF4L2-AS1 (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=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103691883C>G, NC_000023.10:g.102946811C>G, NR_038978.1:n.2197C>G

Select item 14886766005.

rs1488676600 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:103692598 (GRCh38)
X:102947526 (GRCh37)
Canonical SPDI:: NC_000023.11:103692597:G:A
Gene:: MORF4L2-AS1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
G=0./0 (SGDP_PRJ)
A=0.000029/3 (GnomAD)
A=0.00003/8 (TOPMED)
A=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.103692598G>A, NC_000023.10:g.102947526G>A

Select item 14886640786.

rs1488664078 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:103686011 (GRCh38)
X:102940939 (GRCh37)
Canonical SPDI:: NC_000023.11:103686010:T:C
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000023.11:g.103686011T>C, NC_000023.10:g.102940939T>C

Select item 14876916447.

rs1487691644 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:103687355 (GRCh38)
X:102942283 (GRCh37)
Canonical SPDI:: NC_000023.11:103687354:G:A
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.103687355G>A, NC_000023.10:g.102942283G>A, NR_038978.1:n.72G>A

Select item 14872989078.

rs1487298907 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:103687905 (GRCh38)
X:102942833 (GRCh37)
Canonical SPDI:: NC_000023.11:103687904:A:G
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.103687905A>G, NC_000023.10:g.102942833A>G

Select item 14872497739.

rs1487249773 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:103685658 (GRCh38)
X:102940586 (GRCh37)
Canonical SPDI:: NC_000023.11:103685657:A:C
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103685658A>C, NC_000023.10:g.102940586A>C

Select item 148670616110.

rs1486706161 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:103688621 (GRCh38)
X:102943549 (GRCh37)
Canonical SPDI:: NC_000023.11:103688620:G:T
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.103688621G>T, NC_000023.10:g.102943549G>T, NR_038978.1:n.873G>T

Select item 148626577411.

rs1486265774 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:103687012 (GRCh38)
X:102941940 (GRCh37)
Canonical SPDI:: NC_000023.11:103687011:T:G
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103687012T>G, NC_000023.10:g.102941940T>G

Select item 148572490412.

rs1485724904 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:103690443 (GRCh38)
X:102945371 (GRCh37)
Canonical SPDI:: NC_000023.11:103690442:G:A,NC_000023.11:103690442:G:T
Gene:: MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103690443G>A, NC_000023.11:g.103690443G>T, NC_000023.10:g.102945371G>A, NC_000023.10:g.102945371G>T

Select item 148433828713.

rs1484338287 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:103690204 (GRCh38)
X:102945132 (GRCh37)
Canonical SPDI:: NC_000023.11:103690203:A:G
Gene:: MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00003/8 (TOPMED)
G=0.000048/5 (GnomAD)
HGVS:: NC_000023.11:g.103690204A>G, NC_000023.10:g.102945132A>G

Select item 148339727514.

rs1483397275 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:103685289 (GRCh38)
X:102940217 (GRCh37)
Canonical SPDI:: NC_000023.11:103685288:G:A
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.103685289G>A, NC_000023.10:g.102940217G>A

Select item 148300631415.

rs1483006314 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:103685567 (GRCh38)
X:102940495 (GRCh37)
Canonical SPDI:: NC_000023.11:103685566:A:G
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.103685567A>G, NC_000023.10:g.102940495A>G

Select item 148259150616.

rs1482591506 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:103686584 (GRCh38)
X:102941512 (GRCh37)
Canonical SPDI:: NC_000023.11:103686583:G:A
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.103686584G>A, NC_000023.10:g.102941512G>A

Select item 148240504917.

rs1482405049 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:103690416 (GRCh38)
X:102945344 (GRCh37)
Canonical SPDI:: NC_000023.11:103690415:A:G
Gene:: MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103690416A>G, NC_000023.10:g.102945344A>G

Select item 148194530518.

rs1481945305 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: X:103686628 (GRCh38)
X:102941556 (GRCh37)
Canonical SPDI:: NC_000023.11:103686627:A:C
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000023.11:g.103686628A>C, NC_000023.10:g.102941556A>C

Select item 148134879819.

rs1481348798 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:103685445 (GRCh38)
X:102940373 (GRCh37)
Canonical SPDI:: NC_000023.11:103685444:G:A
Gene:: MORF4L2 (Varview), MORF4L2-AS1 (Varview)
Functional Consequence:: intron_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000023/6 (TOPMED)
A=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.103685445G>A, NC_000023.10:g.102940373G>A

Select item 148072402820.

rs1480724028 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:103692725 (GRCh38)
X:102947653 (GRCh37)
Canonical SPDI:: NC_000023.11:103692724:G:C
Gene:: MORF4L2-AS1 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.103692725G>C, NC_000023.10:g.102947653G>C

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