SNP Links for Nucleotide (Select 584458490) - SNP

Links from Nucleotide

Items: 1 to 20 of 34040

<< First< Prev

Page of 1702

Next >Last >>

Select item 14915772171.

rs1491577217 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:35616314 (GRCh38)
6:35584091 (GRCh37)
Canonical SPDI:: NC_000006.12:35616313:CA:
Gene:: FKBP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.35616314_35616315del, NC_000006.11:g.35584091_35584092del, NG_012645.2:g.117269_117270del

Select item 14915737662.

rs1491573766 has merged into rs143946034 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:35578068 (GRCh38)
6:35545845 (GRCh37)
Canonical SPDI:: NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35578055:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FKBP5 (Varview), LOC101929309 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAA=0./0 (ALFA)
AA=0.3293/1649 (1000Genomes)
AA=0.425/17 (GENOME_DK)
HGVS:: NC_000006.12:g.35578068_35578075del, NC_000006.12:g.35578070_35578075del, NC_000006.12:g.35578071_35578075del, NC_000006.12:g.35578072_35578075del, NC_000006.12:g.35578073_35578075del, NC_000006.12:g.35578074_35578075del, NC_000006.12:g.35578075del, NC_000006.12:g.35578075dup, NC_000006.12:g.35578074_35578075dup, NC_000006.12:g.35578073_35578075dup, NC_000006.12:g.35578072_35578075dup, NC_000006.12:g.35578071_35578075dup, NC_000006.11:g.35545845_35545852del, NC_000006.11:g.35545847_35545852del, NC_000006.11:g.35545848_35545852del, NC_000006.11:g.35545849_35545852del, NC_000006.11:g.35545850_35545852del, NC_000006.11:g.35545851_35545852del, NC_000006.11:g.35545852del, NC_000006.11:g.35545852dup, NC_000006.11:g.35545851_35545852dup, NC_000006.11:g.35545850_35545852dup, NC_000006.11:g.35545849_35545852dup, NC_000006.11:g.35545848_35545852dup, NG_012645.2:g.155521_155528del, NG_012645.2:g.155523_155528del, NG_012645.2:g.155524_155528del, NG_012645.2:g.155525_155528del, NG_012645.2:g.155526_155528del, NG_012645.2:g.155527_155528del, NG_012645.2:g.155528del, NG_012645.2:g.155528dup, NG_012645.2:g.155527_155528dup, NG_012645.2:g.155526_155528dup, NG_012645.2:g.155525_155528dup, NG_012645.2:g.155524_155528dup

Select item 14915676493.

rs1491567649 has merged into rs1490454973 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TCC [Show Flanks]
Chromosome:: 6:35726524 (GRCh38)
6:35694302 (GRCh37)
Canonical SPDI:: NC_000006.12:35726524:CTCCTCCTCCTCC:CTCCTCCTCCTCCTCC
Gene:: FKBP5 (Varview), LOC285847 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,downstream_transcript_variant,500B_downstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCCTCCTCCTCCTCC=0./0 (ALFA)
CTC=0.000016/2 (GnomAD)
HGVS:: NC_000006.12:g.35726526TCC[5], NC_000006.11:g.35694303TCC[5], NG_012645.2:g.7048GAG[5]

Select item 14915124904.

rs1491512490 has merged into rs199875825 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTTTTT>-,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:35705262 (GRCh38)
6:35673039 (GRCh37)
Canonical SPDI:: NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35705258:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: FKBP5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTT=0./0 (ALFA)
-=0./0 (Korea1K)
HGVS:: NC_000006.12:g.35705262_35705283del, NC_000006.12:g.35705264_35705283del, NC_000006.12:g.35705266_35705283del, NC_000006.12:g.35705267_35705283del, NC_000006.12:g.35705268_35705283del, NC_000006.12:g.35705269_35705283del, NC_000006.12:g.35705270_35705283del, NC_000006.12:g.35705272_35705283del, NC_000006.12:g.35705273_35705283del, NC_000006.12:g.35705274_35705283del, NC_000006.12:g.35705275_35705283del, NC_000006.12:g.35705276_35705283del, NC_000006.12:g.35705277_35705283del, NC_000006.12:g.35705278_35705283del, NC_000006.12:g.35705279_35705283del, NC_000006.12:g.35705280_35705283del, NC_000006.12:g.35705281_35705283del, NC_000006.12:g.35705282_35705283del, NC_000006.12:g.35705283del, NC_000006.12:g.35705283dup, NC_000006.12:g.35705281_35705283dup, NC_000006.12:g.35705279_35705283dup, NC_000006.11:g.35673039_35673060del, NC_000006.11:g.35673041_35673060del, NC_000006.11:g.35673043_35673060del, NC_000006.11:g.35673044_35673060del, NC_000006.11:g.35673045_35673060del, NC_000006.11:g.35673046_35673060del, NC_000006.11:g.35673047_35673060del, NC_000006.11:g.35673049_35673060del, NC_000006.11:g.35673050_35673060del, NC_000006.11:g.35673051_35673060del, NC_000006.11:g.35673052_35673060del, NC_000006.11:g.35673053_35673060del, NC_000006.11:g.35673054_35673060del, NC_000006.11:g.35673055_35673060del, NC_000006.11:g.35673056_35673060del, NC_000006.11:g.35673057_35673060del, NC_000006.11:g.35673058_35673060del, NC_000006.11:g.35673059_35673060del, NC_000006.11:g.35673060del, NC_000006.11:g.35673060dup, NC_000006.11:g.35673058_35673060dup, NC_000006.11:g.35673056_35673060dup, NG_012645.2:g.28304_28325del, NG_012645.2:g.28306_28325del, NG_012645.2:g.28308_28325del, NG_012645.2:g.28309_28325del, NG_012645.2:g.28310_28325del, NG_012645.2:g.28311_28325del, NG_012645.2:g.28312_28325del, NG_012645.2:g.28314_28325del, NG_012645.2:g.28315_28325del, NG_012645.2:g.28316_28325del, NG_012645.2:g.28317_28325del, NG_012645.2:g.28318_28325del, NG_012645.2:g.28319_28325del, NG_012645.2:g.28320_28325del, NG_012645.2:g.28321_28325del, NG_012645.2:g.28322_28325del, NG_012645.2:g.28323_28325del, NG_012645.2:g.28324_28325del, NG_012645.2:g.28325del, NG_012645.2:g.28325dup, NG_012645.2:g.28323_28325dup, NG_012645.2:g.28321_28325dup

Select item 14914961695.

rs1491496169 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 6:35713077 (GRCh38)
6:35680854 (GRCh37)
Canonical SPDI:: NC_000006.12:35713076:TA:
Gene:: FKBP5 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000006.12:g.35713077_35713078del, NC_000006.11:g.35680854_35680855del, NG_012645.2:g.20506_20507del

Select item 14914325376.

rs1491432537 has merged into rs58812576 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT [Show Flanks]
Chromosome:: 6:35589137 (GRCh38)
6:35556914 (GRCh37)
Canonical SPDI:: NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:35589128:TTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT
Gene:: FKBP5 (Varview), LOC101929309 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.00508/3 (NorthernSweden)
TT=0.4/16 (GENOME_DK)
HGVS:: NC_000006.12:g.35589137_35589141del, NC_000006.12:g.35589138_35589141del, NC_000006.12:g.35589139_35589141del, NC_000006.12:g.35589140_35589141del, NC_000006.12:g.35589141del, NC_000006.12:g.35589141dup, NC_000006.12:g.35589140_35589141dup, NC_000006.12:g.35589139_35589141dup, NC_000006.12:g.35589138_35589141dup, NC_000006.12:g.35589137_35589141dup, NC_000006.12:g.35589136_35589141dup, NC_000006.11:g.35556914_35556918del, NC_000006.11:g.35556915_35556918del, NC_000006.11:g.35556916_35556918del, NC_000006.11:g.35556917_35556918del, NC_000006.11:g.35556918del, NC_000006.11:g.35556918dup, NC_000006.11:g.35556917_35556918dup, NC_000006.11:g.35556916_35556918dup, NC_000006.11:g.35556915_35556918dup, NC_000006.11:g.35556914_35556918dup, NC_000006.11:g.35556913_35556918dup, NG_012645.2:g.144451_144455del, NG_012645.2:g.144452_144455del, NG_012645.2:g.144453_144455del, NG_012645.2:g.144454_144455del, NG_012645.2:g.144455del, NG_012645.2:g.144455dup, NG_012645.2:g.144454_144455dup, NG_012645.2:g.144453_144455dup, NG_012645.2:g.144452_144455dup, NG_012645.2:g.144451_144455dup, NG_012645.2:g.144450_144455dup

Select item 14914235257.

rs1491423525 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 6:35658695 (GRCh38)
6:35626473 (GRCh37)
Canonical SPDI:: NC_000006.12:35658695::T
Gene:: FKBP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: T=0.00017/2 (TOMMO)
T=0.00041/8 (GnomAD)
T=0.00107/1 (Korea1K)
HGVS:: NC_000006.12:g.35658695_35658696insT, NC_000006.11:g.35626472_35626473insT, NG_012645.2:g.74888_74889insA

Select item 14914190588.

rs1491419058 [Homo sapiens]

Variant type:: INS
Alleles:: ->GTT,T,TT,TTT [Show Flanks]
Chromosome:: 6:35573183 (GRCh38)
6:35540961 (GRCh37)
Canonical SPDI:: NC_000006.12:35573183::GTT,NC_000006.12:35573183::T,NC_000006.12:35573183::TT,NC_000006.12:35573183::TTT
Gene:: FKBP5 (Varview), LOC101929309 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
TTT=0.00006/4 (GnomAD)
HGVS:: NC_000006.12:g.35573183_35573184insGTT, NC_000006.12:g.35573183_35573184insT, NC_000006.12:g.35573183_35573184insTT, NC_000006.12:g.35573183_35573184insTTT, NC_000006.11:g.35540960_35540961insGTT, NC_000006.11:g.35540960_35540961insT, NC_000006.11:g.35540960_35540961insTT, NC_000006.11:g.35540960_35540961insTTT, NG_012645.2:g.160400_160401insAAC, NG_012645.2:g.160400_160401insA, NG_012645.2:g.160400_160401insAA, NG_012645.2:g.160400_160401insAAA

Select item 14913750669.

rs1491375066 has merged into rs71002590 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:35693173 (GRCh38)
6:35660950 (GRCh37)
Canonical SPDI:: NC_000006.12:35693163:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:35693163:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:35693163:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:35693163:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:35693163:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:35693163:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:35693163:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35693163:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT
Gene:: FKBP5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
T=0.4579/2293 (1000Genomes)
HGVS:: NC_000006.12:g.35693173_35693180del, NC_000006.12:g.35693179_35693180del, NC_000006.12:g.35693180del, NC_000006.12:g.35693180dup, NC_000006.12:g.35693179_35693180dup, NC_000006.12:g.35693178_35693180dup, NC_000006.12:g.35693177_35693180dup, NC_000006.12:g.35693176_35693180dup, NC_000006.11:g.35660950_35660957del, NC_000006.11:g.35660956_35660957del, NC_000006.11:g.35660957del, NC_000006.11:g.35660957dup, NC_000006.11:g.35660956_35660957dup, NC_000006.11:g.35660955_35660957dup, NC_000006.11:g.35660954_35660957dup, NC_000006.11:g.35660953_35660957dup, NG_012645.2:g.40413_40420del, NG_012645.2:g.40419_40420del, NG_012645.2:g.40420del, NG_012645.2:g.40420dup, NG_012645.2:g.40419_40420dup, NG_012645.2:g.40418_40420dup, NG_012645.2:g.40417_40420dup, NG_012645.2:g.40416_40420dup

Select item 149137462910.

rs1491374629 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:35706424 (GRCh38)
6:35674201 (GRCh37)
Canonical SPDI:: NC_000006.12:35706423:CA:
Gene:: FKBP5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01686/200 (ALFA)
-=0.00182/49 (TOMMO)
HGVS:: NC_000006.12:g.35706424_35706425del, NC_000006.11:g.35674201_35674202del, NG_012645.2:g.27159_27160del

Select item 149136628411.

rs1491366284 has merged into rs34190034 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:35650308 (GRCh38)
6:35618085 (GRCh37)
Canonical SPDI:: NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35650299:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FKBP5 (Varview), LOC124900228 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
A=0.375/15 (GENOME_DK)
A=0.443091/2219 (1000Genomes)
HGVS:: NC_000006.12:g.35650308_35650316del, NC_000006.12:g.35650309_35650316del, NC_000006.12:g.35650311_35650316del, NC_000006.12:g.35650312_35650316del, NC_000006.12:g.35650313_35650316del, NC_000006.12:g.35650314_35650316del, NC_000006.12:g.35650315_35650316del, NC_000006.12:g.35650316del, NC_000006.12:g.35650316dup, NC_000006.12:g.35650315_35650316dup, NC_000006.12:g.35650313_35650316dup, NC_000006.12:g.35650310_35650316dup, NC_000006.11:g.35618085_35618093del, NC_000006.11:g.35618086_35618093del, NC_000006.11:g.35618088_35618093del, NC_000006.11:g.35618089_35618093del, NC_000006.11:g.35618090_35618093del, NC_000006.11:g.35618091_35618093del, NC_000006.11:g.35618092_35618093del, NC_000006.11:g.35618093del, NC_000006.11:g.35618093dup, NC_000006.11:g.35618092_35618093dup, NC_000006.11:g.35618090_35618093dup, NC_000006.11:g.35618087_35618093dup, NG_012645.2:g.83276_83284del, NG_012645.2:g.83277_83284del, NG_012645.2:g.83279_83284del, NG_012645.2:g.83280_83284del, NG_012645.2:g.83281_83284del, NG_012645.2:g.83282_83284del, NG_012645.2:g.83283_83284del, NG_012645.2:g.83284del, NG_012645.2:g.83284dup, NG_012645.2:g.83283_83284dup, NG_012645.2:g.83281_83284dup, NG_012645.2:g.83278_83284dup

Select item 149136383312.

rs1491363833 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>- [Show Flanks]
Chromosome:: 6:35711716 (GRCh38)
6:35679493 (GRCh37)
Canonical SPDI:: NC_000006.12:35711714:ATA:A
Gene:: FKBP5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
-=0.000142/2 (TOMMO)
HGVS:: NC_000006.12:g.35711716_35711717del, NC_000006.11:g.35679493_35679494del, NG_012645.2:g.21868_21869del

Select item 149136089313.

rs1491360893 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:35578055 (GRCh38)
6:35545832 (GRCh37)
Canonical SPDI:: NC_000006.12:35578054:CA:
Gene:: FKBP5 (Varview), LOC101929309 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.06955/825 (ALFA)
-=0.00251/71 (TOMMO)
-=0.01308/23 (Korea1K)
HGVS:: NC_000006.12:g.35578055_35578056del, NC_000006.11:g.35545832_35545833del, NG_012645.2:g.155528_155529del

Select item 149135843014.

rs1491358430 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TA [Show Flanks]
Chromosome:: 6:35687958 (GRCh38)
6:35655736 (GRCh37)
Canonical SPDI:: NC_000006.12:35687958:TATA:TATATA
Gene:: FKBP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATA=0./0 (ALFA)
TA=0.000021/3 (GnomAD)
TA=0.000042/11 (TOPMED)
TA=0.000156/1 (1000Genomes)
HGVS:: NC_000006.12:g.35687959TA[3], NC_000006.11:g.35655736TA[3], NG_012645.2:g.45622TA[3]

Select item 149131526315.

rs1491315263 has merged into rs60390656 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:35696154 (GRCh38)
6:35663931 (GRCh37)
Canonical SPDI:: NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:35696144:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: FKBP5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.004219/2 (NorthernSweden)
HGVS:: NC_000006.12:g.35696154_35696164del, NC_000006.12:g.35696158_35696164del, NC_000006.12:g.35696160_35696164del, NC_000006.12:g.35696161_35696164del, NC_000006.12:g.35696162_35696164del, NC_000006.12:g.35696163_35696164del, NC_000006.12:g.35696164del, NC_000006.12:g.35696164dup, NC_000006.12:g.35696163_35696164dup, NC_000006.12:g.35696162_35696164dup, NC_000006.12:g.35696161_35696164dup, NC_000006.12:g.35696160_35696164dup, NC_000006.11:g.35663931_35663941del, NC_000006.11:g.35663935_35663941del, NC_000006.11:g.35663937_35663941del, NC_000006.11:g.35663938_35663941del, NC_000006.11:g.35663939_35663941del, NC_000006.11:g.35663940_35663941del, NC_000006.11:g.35663941del, NC_000006.11:g.35663941dup, NC_000006.11:g.35663940_35663941dup, NC_000006.11:g.35663939_35663941dup, NC_000006.11:g.35663938_35663941dup, NC_000006.11:g.35663937_35663941dup, NG_012645.2:g.37429_37439del, NG_012645.2:g.37433_37439del, NG_012645.2:g.37435_37439del, NG_012645.2:g.37436_37439del, NG_012645.2:g.37437_37439del, NG_012645.2:g.37438_37439del, NG_012645.2:g.37439del, NG_012645.2:g.37439dup, NG_012645.2:g.37438_37439dup, NG_012645.2:g.37437_37439dup, NG_012645.2:g.37436_37439dup, NG_012645.2:g.37435_37439dup

Select item 149128365916.

rs1491283659 [Homo sapiens]

Variant type:: DEL
Alleles:: GA>- [Show Flanks]
Chromosome:: 6:35573183 (GRCh38)
6:35540960 (GRCh37)
Canonical SPDI:: NC_000006.12:35573182:GA:
Gene:: FKBP5 (Varview), LOC101929309 (Varview)
Functional Consequence:: downstream_transcript_variant,genic_downstream_transcript_variant,intron_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
-=0.00028/8 (TOMMO)
HGVS:: NC_000006.12:g.35573183_35573184del, NC_000006.11:g.35540960_35540961del, NG_012645.2:g.160400_160401del

Select item 149125088417.

rs1491250884 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:35696144 (GRCh38)
6:35663921 (GRCh37)
Canonical SPDI:: NC_000006.12:35696143:CA:
Gene:: FKBP5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00059/7 (ALFA)
HGVS:: NC_000006.12:g.35696144_35696145del, NC_000006.11:g.35663921_35663922del, NG_012645.2:g.37439_37440del

Select item 149124346018.

rs1491243460 has merged into rs35904480 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:35662285 (GRCh38)
6:35630062 (GRCh37)
Canonical SPDI:: NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTT,NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:35662276:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: FKBP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
TT=0.2907/1456 (1000Genomes)
HGVS:: NC_000006.12:g.35662285_35662292del, NC_000006.12:g.35662288_35662292del, NC_000006.12:g.35662289_35662292del, NC_000006.12:g.35662290_35662292del, NC_000006.12:g.35662291_35662292del, NC_000006.12:g.35662292del, NC_000006.12:g.35662292dup, NC_000006.12:g.35662291_35662292dup, NC_000006.12:g.35662284_35662292dup, NC_000006.11:g.35630062_35630069del, NC_000006.11:g.35630065_35630069del, NC_000006.11:g.35630066_35630069del, NC_000006.11:g.35630067_35630069del, NC_000006.11:g.35630068_35630069del, NC_000006.11:g.35630069del, NC_000006.11:g.35630069dup, NC_000006.11:g.35630068_35630069dup, NC_000006.11:g.35630061_35630069dup, NG_012645.2:g.71300_71307del, NG_012645.2:g.71303_71307del, NG_012645.2:g.71304_71307del, NG_012645.2:g.71305_71307del, NG_012645.2:g.71306_71307del, NG_012645.2:g.71307del, NG_012645.2:g.71307dup, NG_012645.2:g.71306_71307dup, NG_012645.2:g.71299_71307dup

Select item 149123813919.

rs1491238139 has merged into rs34841223 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:35707230 (GRCh38)
6:35675007 (GRCh37)
Canonical SPDI:: NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:35707215:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: FKBP5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000006.12:g.35707230_35707233del, NC_000006.12:g.35707231_35707233del, NC_000006.12:g.35707232_35707233del, NC_000006.12:g.35707233del, NC_000006.12:g.35707233dup, NC_000006.12:g.35707232_35707233dup, NC_000006.12:g.35707231_35707233dup, NC_000006.12:g.35707230_35707233dup, NC_000006.12:g.35707229_35707233dup, NC_000006.12:g.35707228_35707233dup, NC_000006.12:g.35707227_35707233dup, NC_000006.12:g.35707226_35707233dup, NC_000006.12:g.35707225_35707233dup, NC_000006.12:g.35707233_35707234insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000006.11:g.35675007_35675010del, NC_000006.11:g.35675008_35675010del, NC_000006.11:g.35675009_35675010del, NC_000006.11:g.35675010del, NC_000006.11:g.35675010dup, NC_000006.11:g.35675009_35675010dup, NC_000006.11:g.35675008_35675010dup, NC_000006.11:g.35675007_35675010dup, NC_000006.11:g.35675006_35675010dup, NC_000006.11:g.35675005_35675010dup, NC_000006.11:g.35675004_35675010dup, NC_000006.11:g.35675003_35675010dup, NC_000006.11:g.35675002_35675010dup, NC_000006.11:g.35675010_35675011insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_012645.2:g.26365_26368del, NG_012645.2:g.26366_26368del, NG_012645.2:g.26367_26368del, NG_012645.2:g.26368del, NG_012645.2:g.26368dup, NG_012645.2:g.26367_26368dup, NG_012645.2:g.26366_26368dup, NG_012645.2:g.26365_26368dup, NG_012645.2:g.26364_26368dup, NG_012645.2:g.26363_26368dup, NG_012645.2:g.26362_26368dup, NG_012645.2:g.26361_26368dup, NG_012645.2:g.26360_26368dup, NG_012645.2:g.26368_26369insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 149120529320.

rs1491205293 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:35650299 (GRCh38)
6:35618076 (GRCh37)
Canonical SPDI:: NC_000006.12:35650298:CA:
Gene:: FKBP5 (Varview), LOC124900228 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000006.12:g.35650299_35650300del, NC_000006.11:g.35618076_35618077del, NG_012645.2:g.83284_83285del

<< First< Prev

Page of 1702

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 34040

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity