SNP Links for Gene (Select 4988) - SNP

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Select item 14915825011.

rs1491582501 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 6:154100143 (GRCh38)
6:154421278 (GRCh37)
Canonical SPDI:: NC_000006.12:154100136:ATATATAT:ATATAT
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: ATATAT=0.00008/1 (ALFA)
-=0.00004/3 (GnomAD)
HGVS:: NC_000006.12:g.154100137AT[3], NC_000006.11:g.154421272AT[3], NG_021208.2:g.94637AT[3]

Select item 14915771172.

rs1491577117 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 6:154152323 (GRCh38)
6:154473458 (GRCh37)
Canonical SPDI:: NC_000006.12:154152321:AGA:A
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.00002/1 (GnomAD)
HGVS:: NC_000006.12:g.154152323_154152324del, NC_000006.11:g.154473458_154473459del, NG_021208.2:g.146823_146824del

Select item 14915569763.

rs1491556976 has merged into rs34724351 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:154152916 (GRCh38)
6:154474051 (GRCh37)
Canonical SPDI:: NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:154152902:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: OPRM1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000006.12:g.154152916_154152919del, NC_000006.12:g.154152917_154152919del, NC_000006.12:g.154152918_154152919del, NC_000006.12:g.154152919del, NC_000006.12:g.154152919dup, NC_000006.12:g.154152918_154152919dup, NC_000006.12:g.154152910_154152919dup, NC_000006.11:g.154474051_154474054del, NC_000006.11:g.154474052_154474054del, NC_000006.11:g.154474053_154474054del, NC_000006.11:g.154474054del, NC_000006.11:g.154474054dup, NC_000006.11:g.154474053_154474054dup, NC_000006.11:g.154474045_154474054dup, NG_021208.2:g.147416_147419del, NG_021208.2:g.147417_147419del, NG_021208.2:g.147418_147419del, NG_021208.2:g.147419del, NG_021208.2:g.147419dup, NG_021208.2:g.147418_147419dup, NG_021208.2:g.147410_147419dup

Select item 14915528754.

rs1491552875 has merged into rs373120574 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:154019757 (GRCh38)
6:154340892 (GRCh37)
Canonical SPDI:: NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:154019747:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.154019757_154019765del, NC_000006.12:g.154019761_154019765del, NC_000006.12:g.154019762_154019765del, NC_000006.12:g.154019763_154019765del, NC_000006.12:g.154019764_154019765del, NC_000006.12:g.154019765del, NC_000006.12:g.154019765dup, NC_000006.12:g.154019764_154019765dup, NC_000006.12:g.154019763_154019765dup, NC_000006.12:g.154019762_154019765dup, NC_000006.12:g.154019761_154019765dup, NC_000006.12:g.154019760_154019765dup, NC_000006.12:g.154019759_154019765dup, NC_000006.12:g.154019758_154019765dup, NC_000006.12:g.154019757_154019765dup, NC_000006.12:g.154019756_154019765dup, NC_000006.12:g.154019755_154019765dup, NC_000006.12:g.154019754_154019765dup, NC_000006.12:g.154019752_154019765dup, NC_000006.12:g.154019751_154019765dup, NC_000006.12:g.154019750_154019765dup, NC_000006.12:g.154019749_154019765dup, NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTTT, NC_000006.12:g.154019765_154019766insTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.154340892_154340900del, NC_000006.11:g.154340896_154340900del, NC_000006.11:g.154340897_154340900del, NC_000006.11:g.154340898_154340900del, NC_000006.11:g.154340899_154340900del, NC_000006.11:g.154340900del, NC_000006.11:g.154340900dup, NC_000006.11:g.154340899_154340900dup, NC_000006.11:g.154340898_154340900dup, NC_000006.11:g.154340897_154340900dup, NC_000006.11:g.154340896_154340900dup, NC_000006.11:g.154340895_154340900dup, NC_000006.11:g.154340894_154340900dup, NC_000006.11:g.154340893_154340900dup, NC_000006.11:g.154340892_154340900dup, NC_000006.11:g.154340891_154340900dup, NC_000006.11:g.154340890_154340900dup, NC_000006.11:g.154340889_154340900dup, NC_000006.11:g.154340887_154340900dup, NC_000006.11:g.154340886_154340900dup, NC_000006.11:g.154340885_154340900dup, NC_000006.11:g.154340884_154340900dup, NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.154340900_154340901insTTTTTTTTTTTTTTTTTTTTTT, NG_021208.2:g.14257_14265del, NG_021208.2:g.14261_14265del, NG_021208.2:g.14262_14265del, NG_021208.2:g.14263_14265del, NG_021208.2:g.14264_14265del, NG_021208.2:g.14265del, NG_021208.2:g.14265dup, NG_021208.2:g.14264_14265dup, NG_021208.2:g.14263_14265dup, NG_021208.2:g.14262_14265dup, NG_021208.2:g.14261_14265dup, NG_021208.2:g.14260_14265dup, NG_021208.2:g.14259_14265dup, NG_021208.2:g.14258_14265dup, NG_021208.2:g.14257_14265dup, NG_021208.2:g.14256_14265dup, NG_021208.2:g.14255_14265dup, NG_021208.2:g.14254_14265dup, NG_021208.2:g.14252_14265dup, NG_021208.2:g.14251_14265dup, NG_021208.2:g.14250_14265dup, NG_021208.2:g.14249_14265dup, NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTT, NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTTT, NG_021208.2:g.14265_14266insTTTTTTTTTTTTTTTTTTTTTT

Select item 14915521075.

rs1491552107 [Homo sapiens]

Variant type:: DEL
Alleles:: GG>- [Show Flanks]
Chromosome:: 6:154152347 (GRCh38)
6:154473482 (GRCh37)
Canonical SPDI:: NC_000006.12:154152346:GG:
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.154152347_154152348del, NC_000006.11:g.154473482_154473483del, NG_021208.2:g.146847_146848del

Select item 14915333626.

rs1491533362 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CA [Show Flanks]
Chromosome:: 6:154238428 (GRCh38)
6:154559563 (GRCh37)
Canonical SPDI:: NC_000006.12:154238428:A:ACA
Gene:: OPRM1 (Varview), IPCEF1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACA=0./0 (ALFA)
AC=0.000004/1 (TOPMED)
AC=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.154238429_154238430insCA, NC_000006.11:g.154559563_154559564insCA, NG_021208.2:g.232929_232930insCA

Select item 14915234337.

rs1491523433 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GAT [Show Flanks]
Chromosome:: 6:154160541 (GRCh38)
6:154481677 (GRCh37)
Canonical SPDI:: NC_000006.12:154160541:GAT:GATGAT
Gene:: OPRM1 (Varview), IPCEF1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GATGAT=0./0 (ALFA)
GAT=0.000021/3 (GnomAD)
GAT=0.000042/11 (TOPMED)
HGVS:: NC_000006.12:g.154160542_154160544dup, NC_000006.11:g.154481677_154481679dup, NG_021208.2:g.155042_155044dup

Select item 14915185708.

rs1491518570 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:154246935 (GRCh38)
6:154568069 (GRCh37)
Canonical SPDI:: NC_000006.12:154246934:CA:
Gene:: OPRM1 (Varview), IPCEF1 (Varview)
Functional Consequence:: intron_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00278/33 (ALFA)
-=0.0006/1 (Korea1K)
HGVS:: NC_000006.12:g.154246935_154246936del, NC_000006.11:g.154568069_154568070del, NG_021208.2:g.241435_241436del

Select item 14915106479.

rs1491510647 [Homo sapiens]

Variant type:: INS
Alleles:: ->GT [Show Flanks]
Chromosome:: 6:154149598 (GRCh38)
6:154470734 (GRCh37)
Canonical SPDI:: NC_000006.12:154149598::GT
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
HGVS:: NC_000006.12:g.154149598_154149599insGT, NC_000006.11:g.154470733_154470734insGT, NG_021208.2:g.144098_144099insGT

Select item 149150057710.

rs1491500577 has merged into rs1194794442 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:154054378 (GRCh38)
6:154375513 (GRCh37)
Canonical SPDI:: NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154054367:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: OPRM1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
AAAAA=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.154054378_154054390del, NC_000006.12:g.154054379_154054390del, NC_000006.12:g.154054380_154054390del, NC_000006.12:g.154054381_154054390del, NC_000006.12:g.154054382_154054390del, NC_000006.12:g.154054383_154054390del, NC_000006.12:g.154054384_154054390del, NC_000006.12:g.154054385_154054390del, NC_000006.12:g.154054386_154054390del, NC_000006.12:g.154054387_154054390del, NC_000006.12:g.154054388_154054390del, NC_000006.12:g.154054389_154054390del, NC_000006.12:g.154054390del, NC_000006.12:g.154054390dup, NC_000006.12:g.154054389_154054390dup, NC_000006.12:g.154054388_154054390dup, NC_000006.12:g.154054387_154054390dup, NC_000006.12:g.154054386_154054390dup, NC_000006.12:g.154054385_154054390dup, NC_000006.11:g.154375513_154375525del, NC_000006.11:g.154375514_154375525del, NC_000006.11:g.154375515_154375525del, NC_000006.11:g.154375516_154375525del, NC_000006.11:g.154375517_154375525del, NC_000006.11:g.154375518_154375525del, NC_000006.11:g.154375519_154375525del, NC_000006.11:g.154375520_154375525del, NC_000006.11:g.154375521_154375525del, NC_000006.11:g.154375522_154375525del, NC_000006.11:g.154375523_154375525del, NC_000006.11:g.154375524_154375525del, NC_000006.11:g.154375525del, NC_000006.11:g.154375525dup, NC_000006.11:g.154375524_154375525dup, NC_000006.11:g.154375523_154375525dup, NC_000006.11:g.154375522_154375525dup, NC_000006.11:g.154375521_154375525dup, NC_000006.11:g.154375520_154375525dup, NG_021208.2:g.48878_48890del, NG_021208.2:g.48879_48890del, NG_021208.2:g.48880_48890del, NG_021208.2:g.48881_48890del, NG_021208.2:g.48882_48890del, NG_021208.2:g.48883_48890del, NG_021208.2:g.48884_48890del, NG_021208.2:g.48885_48890del, NG_021208.2:g.48886_48890del, NG_021208.2:g.48887_48890del, NG_021208.2:g.48888_48890del, NG_021208.2:g.48889_48890del, NG_021208.2:g.48890del, NG_021208.2:g.48890dup, NG_021208.2:g.48889_48890dup, NG_021208.2:g.48888_48890dup, NG_021208.2:g.48887_48890dup, NG_021208.2:g.48886_48890dup, NG_021208.2:g.48885_48890dup

Select item 149149102211.

rs1491491022 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CAA,CACAA,CACACAA,CACACACAA [Show Flanks]
Chromosome:: 6:154198663 (GRCh38)
6:154519798 (GRCh37)
Canonical SPDI:: NC_000006.12:154198663:A:ACAA,NC_000006.12:154198663:A:ACACAA,NC_000006.12:154198663:A:ACACACAA,NC_000006.12:154198663:A:ACACACACAA
Gene:: OPRM1 (Varview), IPCEF1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACAA=0./0 (ALFA)
ACACA=0.00007/1 (TOMMO)
HGVS:: NC_000006.12:g.154198664_154198665insCAA, NC_000006.12:g.154198664AC[2]AA[1], NC_000006.12:g.154198664AC[3]AA[1], NC_000006.12:g.154198664AC[4]AA[1], NC_000006.11:g.154519798_154519799insCAA, NC_000006.11:g.154519798AC[2]AA[1], NC_000006.11:g.154519798AC[3]AA[1], NC_000006.11:g.154519798AC[4]AA[1], NG_021208.2:g.193164_193165insCAA, NG_021208.2:g.193164AC[2]AA[1], NG_021208.2:g.193164AC[3]AA[1], NG_021208.2:g.193164AC[4]AA[1]

Select item 149148760212.

rs1491487602 has merged into rs11289794 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA [Show Flanks]
Chromosome:: 6:154227996 (GRCh38)
6:154549130 (GRCh37)
Canonical SPDI:: NC_000006.12:154227987:AAAAAAAAAA:AAAAAAAA,NC_000006.12:154227987:AAAAAAAAAA:AAAAAAAAA,NC_000006.12:154227987:AAAAAAAAAA:AAAAAAAAAAA
Gene:: OPRM1 (Varview), IPCEF1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0.419008/3699 (ALFA)
A=0.251092/460 (Korea1K)
A=0.314647/1576 (1000Genomes)
A=0.405943/107449 (TOPMED)
A=0.443923/1987 (Estonian)
A=0.459782/1772 (ALSPAC)
A=0.462513/1715 (TWINSUK)
A=0.472946/472 (GoNL)
-=0.489967/293 (NorthernSweden)
A=0.5/20 (GENOME_DK)
HGVS:: NC_000006.12:g.154227996_154227997del, NC_000006.12:g.154227997del, NC_000006.12:g.154227997dup, NC_000006.11:g.154549130_154549131del, NC_000006.11:g.154549131del, NC_000006.11:g.154549131dup, NG_021208.2:g.222496_222497del, NG_021208.2:g.222497del, NG_021208.2:g.222497dup

Select item 149147821413.

rs1491478214 [Homo sapiens]

Variant type:: INS
Alleles:: ->G,GAAAGAGAGAG [Show Flanks]
Chromosome:: 6:154099368 (GRCh38)
6:154420504 (GRCh37)
Canonical SPDI:: NC_000006.12:154099368::G,NC_000006.12:154099368::GAAAGAGAGAG
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAAAGAGAGAG=0./0 (ALFA)
G=0.00017/3 (TOMMO)
HGVS:: NC_000006.12:g.154099368_154099369insG, NC_000006.12:g.154099368_154099369insGAAAGAGAGAG, NC_000006.11:g.154420503_154420504insG, NC_000006.11:g.154420503_154420504insGAAAGAGAGAG, NG_021208.2:g.93868_93869insG, NG_021208.2:g.93868_93869insGAAAGAGAGAG

Select item 149147814814.

rs1491478148 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATTT [Show Flanks]
Chromosome:: 6:154140333 (GRCh38)
6:154461469 (GRCh37)
Canonical SPDI:: NC_000006.12:154140333:TTT:TTTATTT
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTTATTT=0./0 (ALFA)
TTTA=0.00001/1 (GnomAD)
HGVS:: NC_000006.12:g.154140336_154140337insATTT, NC_000006.11:g.154461471_154461472insATTT, NG_021208.2:g.134836_134837insATTT

Select item 149147526715.

rs1491475267 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATA,ATATATATATATATATATA,ATATATATATATATATATATA,ATATATATATATC [Show Flanks]
Chromosome:: 6:154180415 (GRCh38)
6:154501550 (GRCh37)
Canonical SPDI:: NC_000006.12:154180415::A,NC_000006.12:154180415::ATA,NC_000006.12:154180415::ATATA,NC_000006.12:154180415::ATATATA,NC_000006.12:154180415::ATATATATA,NC_000006.12:154180415::ATATATATATA,NC_000006.12:154180415::ATATATATATATA,NC_000006.12:154180415::ATATATATATATATA,NC_000006.12:154180415::ATATATATATATATATA,NC_000006.12:154180415::ATATATATATATATATATA,NC_000006.12:154180415::ATATATATATATATATATATA,NC_000006.12:154180415::ATATATATATATC
Gene:: OPRM1 (Varview), IPCEF1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
A=0.0042/26 (TOMMO)
HGVS:: NC_000006.12:g.154180415_154180416insA, NC_000006.12:g.154180415_154180416insATA, NC_000006.12:g.154180415_154180416insATATA, NC_000006.12:g.154180415_154180416insATATATA, NC_000006.12:g.154180415_154180416insATATATATA, NC_000006.12:g.154180415_154180416insATATATATATA, NC_000006.12:g.154180415_154180416insATATATATATATA, NC_000006.12:g.154180415_154180416insATATATATATATATA, NC_000006.12:g.154180415_154180416insATATATATATATATATA, NC_000006.12:g.154180415_154180416insATATATATATATATATATA, NC_000006.12:g.154180415_154180416insATATATATATATATATATATA, NC_000006.12:g.154180415_154180416insATATATATATATC, NC_000006.11:g.154501549_154501550insA, NC_000006.11:g.154501549_154501550insATA, NC_000006.11:g.154501549_154501550insATATA, NC_000006.11:g.154501549_154501550insATATATA, NC_000006.11:g.154501549_154501550insATATATATA, NC_000006.11:g.154501549_154501550insATATATATATA, NC_000006.11:g.154501549_154501550insATATATATATATA, NC_000006.11:g.154501549_154501550insATATATATATATATA, NC_000006.11:g.154501549_154501550insATATATATATATATATA, NC_000006.11:g.154501549_154501550insATATATATATATATATATA, NC_000006.11:g.154501549_154501550insATATATATATATATATATATA, NC_000006.11:g.154501549_154501550insATATATATATATC, NG_021208.2:g.174915_174916insA, NG_021208.2:g.174915_174916insATA, NG_021208.2:g.174915_174916insATATA, NG_021208.2:g.174915_174916insATATATA, NG_021208.2:g.174915_174916insATATATATA, NG_021208.2:g.174915_174916insATATATATATA, NG_021208.2:g.174915_174916insATATATATATATA, NG_021208.2:g.174915_174916insATATATATATATATA, NG_021208.2:g.174915_174916insATATATATATATATATA, NG_021208.2:g.174915_174916insATATATATATATATATATA, NG_021208.2:g.174915_174916insATATATATATATATATATATA, NG_021208.2:g.174915_174916insATATATATATATC

Select item 149147436716.

rs1491474367 has merged into rs10692865 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAGAAAAG>-,AAAAG,AAAAGAAAAGAAAAG,AAAAGAAAAGAAAAGAAAAG,AAAAGAAAAGAAAAGAAAAGAAAAG [Show Flanks]
Chromosome:: 6:154242897 (GRCh38)
6:154564031 (GRCh37)
Canonical SPDI:: NC_000006.12:154242887:AAAGAAAAGAAAAGAAAAG:AAAGAAAAG,NC_000006.12:154242887:AAAGAAAAGAAAAGAAAAG:AAAGAAAAGAAAAG,NC_000006.12:154242887:AAAGAAAAGAAAAGAAAAG:AAAGAAAAGAAAAGAAAAGAAAAG,NC_000006.12:154242887:AAAGAAAAGAAAAGAAAAG:AAAGAAAAGAAAAGAAAAGAAAAGAAAAG,NC_000006.12:154242887:AAAGAAAAGAAAAGAAAAG:AAAGAAAAGAAAAGAAAAGAAAAGAAAAGAAAAG
Gene:: OPRM1 (Varview), IPCEF1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAGAAAAGAAAAGAAAAGAAAAGAAAAGAAAAG=0./0 (ALFA)
AAAGA=0.0413/120 (1000Genomes)
HGVS:: NC_000006.12:g.154242892AAAAG[1], NC_000006.12:g.154242892AAAAG[2], NC_000006.12:g.154242892AAAAG[4], NC_000006.12:g.154242892AAAAG[5], NC_000006.12:g.154242892AAAAG[6], NC_000006.11:g.154564026AAAAG[1], NC_000006.11:g.154564026AAAAG[2], NC_000006.11:g.154564026AAAAG[4], NC_000006.11:g.154564026AAAAG[5], NC_000006.11:g.154564026AAAAG[6], NG_021208.2:g.237392AAAAG[1], NG_021208.2:g.237392AAAAG[2], NG_021208.2:g.237392AAAAG[4], NG_021208.2:g.237392AAAAG[5], NG_021208.2:g.237392AAAAG[6]

Select item 149146543517.

rs1491465435 has merged into rs58367883 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:154144760 (GRCh38)
6:154465895 (GRCh37)
Canonical SPDI:: NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:154144748:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: OPRM1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000006.12:g.154144760_154144772del, NC_000006.12:g.154144761_154144772del, NC_000006.12:g.154144762_154144772del, NC_000006.12:g.154144763_154144772del, NC_000006.12:g.154144765_154144772del, NC_000006.12:g.154144766_154144772del, NC_000006.12:g.154144767_154144772del, NC_000006.12:g.154144768_154144772del, NC_000006.12:g.154144769_154144772del, NC_000006.12:g.154144770_154144772del, NC_000006.12:g.154144771_154144772del, NC_000006.12:g.154144772del, NC_000006.12:g.154144772dup, NC_000006.12:g.154144771_154144772dup, NC_000006.12:g.154144770_154144772dup, NC_000006.12:g.154144769_154144772dup, NC_000006.12:g.154144768_154144772dup, NC_000006.12:g.154144767_154144772dup, NC_000006.12:g.154144766_154144772dup, NC_000006.12:g.154144765_154144772dup, NC_000006.12:g.154144761_154144772dup, NC_000006.12:g.154144760_154144772dup, NC_000006.12:g.154144749_154144772dup, NC_000006.12:g.154144772_154144773insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.154144772_154144773insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.154144772_154144773insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.154465895_154465907del, NC_000006.11:g.154465896_154465907del, NC_000006.11:g.154465897_154465907del, NC_000006.11:g.154465898_154465907del, NC_000006.11:g.154465900_154465907del, NC_000006.11:g.154465901_154465907del, NC_000006.11:g.154465902_154465907del, NC_000006.11:g.154465903_154465907del, NC_000006.11:g.154465904_154465907del, NC_000006.11:g.154465905_154465907del, NC_000006.11:g.154465906_154465907del, NC_000006.11:g.154465907del, NC_000006.11:g.154465907dup, NC_000006.11:g.154465906_154465907dup, NC_000006.11:g.154465905_154465907dup, NC_000006.11:g.154465904_154465907dup, NC_000006.11:g.154465903_154465907dup, NC_000006.11:g.154465902_154465907dup, NC_000006.11:g.154465901_154465907dup, NC_000006.11:g.154465900_154465907dup, NC_000006.11:g.154465896_154465907dup, NC_000006.11:g.154465895_154465907dup, NC_000006.11:g.154465884_154465907dup, NC_000006.11:g.154465907_154465908insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.154465907_154465908insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.154465907_154465908insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_021208.2:g.139260_139272del, NG_021208.2:g.139261_139272del, NG_021208.2:g.139262_139272del, NG_021208.2:g.139263_139272del, NG_021208.2:g.139265_139272del, NG_021208.2:g.139266_139272del, NG_021208.2:g.139267_139272del, NG_021208.2:g.139268_139272del, NG_021208.2:g.139269_139272del, NG_021208.2:g.139270_139272del, NG_021208.2:g.139271_139272del, NG_021208.2:g.139272del, NG_021208.2:g.139272dup, NG_021208.2:g.139271_139272dup, NG_021208.2:g.139270_139272dup, NG_021208.2:g.139269_139272dup, NG_021208.2:g.139268_139272dup, NG_021208.2:g.139267_139272dup, NG_021208.2:g.139266_139272dup, NG_021208.2:g.139265_139272dup, NG_021208.2:g.139261_139272dup, NG_021208.2:g.139260_139272dup, NG_021208.2:g.139249_139272dup, NG_021208.2:g.139272_139273insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_021208.2:g.139272_139273insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_021208.2:g.139272_139273insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149146489618.

rs1491464896 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 6:154099896 (GRCh38)
6:154421031 (GRCh37)
Canonical SPDI:: NC_000006.12:154099895:TT:
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
HGVS:: NC_000006.12:g.154099896_154099897del, NC_000006.11:g.154421031_154421032del, NG_021208.2:g.94396_94397del

Select item 149146093819.

rs1491460938 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:154110886 (GRCh38)
6:154432021 (GRCh37)
Canonical SPDI:: NC_000006.12:154110885:CA:
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000006.12:g.154110886_154110887del, NC_000006.11:g.154432021_154432022del, NG_021208.2:g.105386_105387del

Select item 149146069820.

rs1491460698 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>-,GAGA [Show Flanks]
Chromosome:: 6:154152339 (GRCh38)
6:154473474 (GRCh37)
Canonical SPDI:: NC_000006.12:154152337:AGA:A,NC_000006.12:154152337:AGA:AGAGA
Gene:: OPRM1 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: AGAGA=0./0 (ALFA)
-=0.00025/3 (GnomAD)
HGVS:: NC_000006.12:g.154152339_154152340del, NC_000006.12:g.154152339_154152340dup, NC_000006.11:g.154473474_154473475del, NC_000006.11:g.154473474_154473475dup, NG_021208.2:g.146839_146840del, NG_021208.2:g.146839_146840dup

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