SNP Links for Gene (Select 7175) - SNP

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14915863851.

rs1491586385 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AACATATATA,AATA,AATATATA,AATATATATA,ATA,ATTA [Show Flanks]
Chromosome:: 1:186327199 (GRCh38)
1:186296332 (GRCh37)
Canonical SPDI:: NC_000001.11:186327199::A,NC_000001.11:186327199::AACATATATA,NC_000001.11:186327199::AATA,NC_000001.11:186327199::AATATATA,NC_000001.11:186327199::AATATATATA,NC_000001.11:186327199::ATA,NC_000001.11:186327199::ATTA
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AATA=0./0 (ALFA)
HGVS:: NC_000001.11:g.186327199_186327200insA, NC_000001.11:g.186327199_186327200insAACATATATA, NC_000001.11:g.186327199_186327200insAATA, NC_000001.11:g.186327199_186327200insAATATATA, NC_000001.11:g.186327199_186327200insAATATATATA, NC_000001.11:g.186327199_186327200insATA, NC_000001.11:g.186327199_186327200insATTA, NC_000001.10:g.186296331_186296332insA, NC_000001.10:g.186296331_186296332insAACATATATA, NC_000001.10:g.186296331_186296332insAATA, NC_000001.10:g.186296331_186296332insAATATATA, NC_000001.10:g.186296331_186296332insAATATATATA, NC_000001.10:g.186296331_186296332insATA, NC_000001.10:g.186296331_186296332insATTA, NG_023284.1:g.53126_53127insT, NG_023284.1:g.53126_53127insTATATATGTT, NG_023284.1:g.53126_53127insTATT, NG_023284.1:g.53126_53127insTATATATT, NG_023284.1:g.53126_53127insTATATATATT, NG_023284.1:g.53126_53127insTAT, NG_023284.1:g.53126_53127insTAAT

Select item 14915852242.

rs1491585224 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 1:186327235 (GRCh38)
1:186296368 (GRCh37)
Canonical SPDI:: NC_000001.11:186327235::A
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.03861/458 (ALFA)
A=0.00465/95 (GnomAD)
A=0.01347/108 (TOMMO)
HGVS:: NC_000001.11:g.186327235_186327236insA, NC_000001.10:g.186296367_186296368insA, NG_023284.1:g.53090_53091insT

Select item 14915838453.

rs1491583845 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 1:186327051 (GRCh38)
1:186296184 (GRCh37)
Canonical SPDI:: NC_000001.11:186327051::T
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.186327051_186327052insT, NC_000001.10:g.186296183_186296184insT, NG_023284.1:g.53274_53275insA

Select item 14914933564.

rs1491493356 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AA,AAA,AAATA,AAATATA,AAATATATAA,AAATATATATATATAAATATATATAAATATATATATATATAAATATATATAAATATATAA,AAATATATATATATATAAAAATATATATAAATATATAATATATATTTATATATATAATATATATAAATATATAA,AAATATATATATATATAAATATATATAAATATATAA,AAATATATATATATATAAATATATATAAATATATAATATATATATATATAATATATATAAATATATAA,AAATATATATATATATATAAATATATATAAATATATAA,AAATATGTAA,AATATATAA,ACATATATAA,ACGTA,ATAA,ATATAAATATATATAAATATATATATATATAAATATATATAAATATATAA,ATATATTTATATATATAATATATATAAATATATAA [Show Flanks]
Chromosome:: 1:186327192 (GRCh38)
1:186296325 (GRCh37)
Canonical SPDI:: NC_000001.11:186327192::A,NC_000001.11:186327192::AA,NC_000001.11:186327192::AAA,NC_000001.11:186327192::AAATA,NC_000001.11:186327192::AAATATA,NC_000001.11:186327192::AAATATATAA,NC_000001.11:186327192::AAATATATATATATAAATATATATAAATATATATATATATAAATATATATAAATATATAA,NC_000001.11:186327192::AAATATATATATATATAAAAATATATATAAATATATAATATATATTTATATATATAATATATATAAATATATAA,NC_000001.11:186327192::AAATATATATATATATAAATATATATAAATATATAA,NC_000001.11:186327192::AAATATATATATATATAAATATATATAAATATATAATATATATATATATAATATATATAAATATATAA,NC_000001.11:186327192::AAATATATATATATATATAAATATATATAAATATATAA,NC_000001.11:186327192::AAATATGTAA,NC_000001.11:186327192::AATATATAA,NC_000001.11:186327192::ACATATATAA,NC_000001.11:186327192::ACGTA,NC_000001.11:186327192::ATAA,NC_000001.11:186327192::ATATAAATATATATAAATATATATATATATAAATATATATAAATATATAA,NC_000001.11:186327192::ATATATTTATATATATAATATATATAAATATATAA
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
AAATATATATATATATATAAATATATATAAATATATAA=0.01778/56 (TOMMO)
HGVS:: NC_000001.11:g.186327192_186327193insA, NC_000001.11:g.186327192_186327193insAA, NC_000001.11:g.186327192_186327193insAAA, NC_000001.11:g.186327192_186327193insAAATA, NC_000001.11:g.186327192_186327193insAAATATA, NC_000001.11:g.186327192_186327193insAAATATATAA, NC_000001.11:g.186327192_186327193insAAATATATATATATAAATATATATAAATATATATATATATAAATATATATAAATATATAA, NC_000001.11:g.186327192_186327193insAAATATATATATATATAAAAATATATATAAATATATAATATATATTTATATATATAATATATATAAATATATAA, NC_000001.11:g.186327192_186327193insAAATATATATATATATAAATATATATAAATATATAA, NC_000001.11:g.186327192_186327193insAAATATATATATATATAAATATATATAAATATATAATATATATATATATAATATATATAAATATATAA, NC_000001.11:g.186327192_186327193insAAATATATATATATATATAAATATATATAAATATATAA, NC_000001.11:g.186327192_186327193insAAATATGTAA, NC_000001.11:g.186327192_186327193insAATATATAA, NC_000001.11:g.186327192_186327193insACATATATAA, NC_000001.11:g.186327192_186327193insACGTA, NC_000001.11:g.186327192_186327193insATAA, NC_000001.11:g.186327192_186327193insATATAAATATATATAAATATATATATATATAAATATATATAAATATATAA, NC_000001.11:g.186327192_186327193insATATATTTATATATATAATATATATAAATATATAA, NC_000001.10:g.186296324_186296325insA, NC_000001.10:g.186296324_186296325insAA, NC_000001.10:g.186296324_186296325insAAA, NC_000001.10:g.186296324_186296325insAAATA, NC_000001.10:g.186296324_186296325insAAATATA, NC_000001.10:g.186296324_186296325insAAATATATAA, NC_000001.10:g.186296324_186296325insAAATATATATATATAAATATATATAAATATATATATATATAAATATATATAAATATATAA, NC_000001.10:g.186296324_186296325insAAATATATATATATATAAAAATATATATAAATATATAATATATATTTATATATATAATATATATAAATATATAA, NC_000001.10:g.186296324_186296325insAAATATATATATATATAAATATATATAAATATATAA, NC_000001.10:g.186296324_186296325insAAATATATATATATATAAATATATATAAATATATAATATATATATATATAATATATATAAATATATAA, NC_000001.10:g.186296324_186296325insAAATATATATATATATATAAATATATATAAATATATAA, NC_000001.10:g.186296324_186296325insAAATATGTAA, NC_000001.10:g.186296324_186296325insAATATATAA, NC_000001.10:g.186296324_186296325insACATATATAA, NC_000001.10:g.186296324_186296325insACGTA, NC_000001.10:g.186296324_186296325insATAA, NC_000001.10:g.186296324_186296325insATATAAATATATATAAATATATATATATATAAATATATATAAATATATAA, NC_000001.10:g.186296324_186296325insATATATTTATATATATAATATATATAAATATATAA, NG_023284.1:g.53133_53134insT, NG_023284.1:g.53133_53134insTT, NG_023284.1:g.53133_53134insTTT, NG_023284.1:g.53133_53134insTATTT, NG_023284.1:g.53133_53134insTATATTT, NG_023284.1:g.53133_53134insTTATATATTT, NG_023284.1:g.53133_53134insTTATATATTTATATATATTTATATATATATATATTTATATATATTTATATATATATATTT, NG_023284.1:g.53133_53134insTTATATATTTATATATATTATATATATAAATATATATTATATATTTATATATATTTTTATATATATATATATTT, NG_023284.1:g.53133_53134insTTATATATTTATATATATTTATATATATATATATTT, NG_023284.1:g.53133_53134insTTATATATTTATATATATTATATATATATATATTATATATTTATATATATTTATATATATATATATTT, NG_023284.1:g.53133_53134insTTATATATTTATATATATTTATATATATATATATATTT, NG_023284.1:g.53133_53134insTTACATATTT, NG_023284.1:g.53133_53134insTTATATATT, NG_023284.1:g.53133_53134insTTATATATGT, NG_023284.1:g.53133_53134insTACGT, NG_023284.1:g.53133_53134insTTAT, NG_023284.1:g.53133_53134insTTATATATTTATATATATTTATATATATATATATTTATATATATTTATAT, NG_023284.1:g.53133_53134insTTATATATTTATATATATTATATATATAAATATAT

Select item 14914778705.

rs1491477870 has merged into rs1394788844 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>-,ATAT [Show Flanks]
Chromosome:: 1:186327234 (GRCh38)
1:186296366 (GRCh37)
Canonical SPDI:: NC_000001.11:186327227:ATATATAT:ATATAT,NC_000001.11:186327227:ATATATAT:ATATATATAT
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATATAT=0./0 (ALFA)
-=0.00309/44 (GnomAD)
HGVS:: NC_000001.11:g.186327228AT[3], NC_000001.11:g.186327228AT[5], NC_000001.10:g.186296360AT[3], NC_000001.10:g.186296360AT[5], NG_023284.1:g.53091AT[3], NG_023284.1:g.53091AT[5]

Select item 14914748826.

rs1491474882 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:186327165 (GRCh38)
1:186296297 (GRCh37)
Canonical SPDI:: NC_000001.11:186327163:ACA:A
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00261/31 (ALFA)
-=0.00214/11 (TOMMO)
-=0.02876/13 (GnomAD)
HGVS:: NC_000001.11:g.186327165_186327166del, NC_000001.10:g.186296297_186296298del, NG_023284.1:g.53161_53162del

Select item 14914602437.

rs1491460243 has merged into rs1430573556 [Homo sapiens]

Variant type:: DELINS
Alleles:: TAAATATATA>-,TAAATATATATAAATATATA [Show Flanks]
Chromosome:: 1:186327116 (GRCh38)
1:186296248 (GRCh37)
Canonical SPDI:: NC_000001.11:186327098:ATATATATAAATATATATAAATATATA:ATATATATAAATATATA,NC_000001.11:186327098:ATATATATAAATATATATAAATATATA:ATATATATAAATATATATAAATATATATAAATATATA
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ATATATATAAATATATATAAATATATATAAATATATA=0./0 (ALFA)
HGVS:: NC_000001.11:g.186327106TAAATATATA[1], NC_000001.11:g.186327106TAAATATATA[3], NC_000001.10:g.186296238TAAATATATA[1], NC_000001.10:g.186296238TAAATATATA[3], NG_023284.1:g.53208TTATATATAT[1], NG_023284.1:g.53208TTATATATAT[3]

Select item 14914561768.

rs1491456176 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTATATA [Show Flanks]
Chromosome:: 1:186327314 (GRCh38)
1:186296447 (GRCh37)
Canonical SPDI:: NC_000001.11:186327314:A:ACTATATA
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ACTATATA=0./0 (ALFA)
HGVS:: NC_000001.11:g.186327315_186327316insCTATATA, NC_000001.10:g.186296447_186296448insCTATATA, NG_023284.1:g.53011TA[3]GT[1]

Select item 14914372099.

rs1491437209 [Homo sapiens]

Variant type:: INS
Alleles:: ->TATATAAATATATATAAATATATAATATATATT,TATATATT,TATATT [Show Flanks]
Chromosome:: 1:186327164 (GRCh38)
1:186296297 (GRCh37)
Canonical SPDI:: NC_000001.11:186327164::TATATAAATATATATAAATATATAATATATATT,NC_000001.11:186327164::TATATATT,NC_000001.11:186327164::TATATT
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATT=0./0 (ALFA)
TATATAAATATATATAAATATATAATATATATT=0.00008/0 (TOMMO)
HGVS:: NC_000001.11:g.186327164_186327165insTATATAAATATATATAAATATATAATATATATT, NC_000001.11:g.186327164_186327165insTATATATT, NC_000001.11:g.186327164_186327165insTATATT, NC_000001.10:g.186296296_186296297insTATATAAATATATATAAATATATAATATATATT, NC_000001.10:g.186296296_186296297insTATATATT, NC_000001.10:g.186296296_186296297insTATATT, NG_023284.1:g.53161_53162insAATATATATTATATATTTATATATATTTATATA, NG_023284.1:g.53161_53162insAATATATA, NG_023284.1:g.53161_53162insAATATA

Select item 149143686310.

rs1491436863 has merged into rs1233124933 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T [Show Flanks]
Chromosome:: 1:186327236 (GRCh38)
1:186296368 (GRCh37)
Canonical SPDI:: NC_000001.11:186327234:TTT:T,NC_000001.11:186327234:TTT:TT
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.00004/1 (GnomAD)
-=0.00235/28 (TOMMO)
HGVS:: NC_000001.11:g.186327236_186327237del, NC_000001.11:g.186327237del, NC_000001.10:g.186296368_186296369del, NC_000001.10:g.186296369del, NG_023284.1:g.53090_53091del, NG_023284.1:g.53091del

Select item 149143291611.

rs1491432916 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TT,TTT [Show Flanks]
Chromosome:: 1:186327087 (GRCh38)
1:186296220 (GRCh37)
Canonical SPDI:: NC_000001.11:186327087::T,NC_000001.11:186327087::TT,NC_000001.11:186327087::TTT
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
HGVS:: NC_000001.11:g.186327087_186327088insT, NC_000001.11:g.186327087_186327088insTT, NC_000001.11:g.186327087_186327088insTTT, NC_000001.10:g.186296219_186296220insT, NC_000001.10:g.186296219_186296220insTT, NC_000001.10:g.186296219_186296220insTTT, NG_023284.1:g.53238_53239insA, NG_023284.1:g.53238_53239insAA, NG_023284.1:g.53238_53239insAAA

Select item 149139333512.

rs1491393335 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATATAAATATATATAAATATA,ATATATAAATATATATAAATATATAATATATATA,ATATATAATATATATAAATATA [Show Flanks]
Chromosome:: 1:186327273 (GRCh38)
1:186296406 (GRCh37)
Canonical SPDI:: NC_000001.11:186327273::A,NC_000001.11:186327273::ATATAAATATATATAAATATA,NC_000001.11:186327273::ATATATAAATATATATAAATATATAATATATATA,NC_000001.11:186327273::ATATATAATATATATAAATATA
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00009/1 (ALFA)
ATATATAAATATATATAAATATATAATATATATA=0.0003/2 (GnomAD)
ATATATAATATATATAAATATA=0.00047/3 (1000Genomes)
HGVS:: NC_000001.11:g.186327273_186327274insA, NC_000001.11:g.186327273_186327274insATATAAATATATATAAATATA, NC_000001.11:g.186327273_186327274insATATATAAATATATATAAATATATAATATATATA, NC_000001.11:g.186327273_186327274insATATATAATATATATAAATATA, NC_000001.10:g.186296405_186296406insA, NC_000001.10:g.186296405_186296406insATATAAATATATATAAATATA, NC_000001.10:g.186296405_186296406insATATATAAATATATATAAATATATAATATATATA, NC_000001.10:g.186296405_186296406insATATATAATATATATAAATATA, NG_023284.1:g.53052_53053insT, NG_023284.1:g.53052_53053insTATATTTATATATATTTATAT, NG_023284.1:g.53052_53053insTATATATATTATATATTTATATATATTTATATAT, NG_023284.1:g.53052_53053insTATATTTATATATATTATATAT

Select item 149136756813.

rs1491367568 has merged into rs1292534497 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATA>-,TA [Show Flanks]
Chromosome:: 1:186327207 (GRCh38)
1:186296339 (GRCh37)
Canonical SPDI:: NC_000001.11:186327200:TATATATATA:TATATA,NC_000001.11:186327200:TATATATATA:TATATATA
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATA=0./0 (ALFA)
-=0.00008/2 (TOMMO)
HGVS:: NC_000001.11:g.186327201TA[3], NC_000001.11:g.186327201TA[4], NC_000001.10:g.186296333TA[3], NC_000001.10:g.186296333TA[4], NG_023284.1:g.53116TA[3], NG_023284.1:g.53116TA[4]

Select item 149136494014.

rs1491364940 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TATATATAA [Show Flanks]
Chromosome:: 1:186327174 (GRCh38)
1:186296307 (GRCh37)
Canonical SPDI:: NC_000001.11:186327174:ATATATATAA:ATATATATAATATATATAA
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ATATATATAATATATATAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.186327176_186327184dup, NC_000001.10:g.186296308_186296316dup, NG_023284.1:g.53143_53151dup

Select item 149136248815.

rs1491362488 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 1:186327227 (GRCh38)
1:186296359 (GRCh37)
Canonical SPDI:: NC_000001.11:186327226:AA:
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00003/1 (GnomAD)
-=0.0003/3 (TOMMO)
HGVS:: NC_000001.11:g.186327227_186327228del, NC_000001.10:g.186296359_186296360del, NG_023284.1:g.53098_53099del

Select item 149133562516.

rs1491335625 has merged into rs1018261043 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>-,GAGA [Show Flanks]
Chromosome:: 1:186323609 (GRCh38)
1:186292741 (GRCh37)
Canonical SPDI:: NC_000001.11:186323597:AGAGAGAGAGAGA:AGAGAGAGAGA,NC_000001.11:186323597:AGAGAGAGAGAGA:AGAGAGAGAGAGAGA
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAGAGAGAGAGAGA=0./0 (ALFA)
AG=0.000029/4 (GnomAD)
HGVS:: NC_000001.11:g.186323599GA[5], NC_000001.11:g.186323599GA[7], NC_000001.10:g.186292731GA[5], NC_000001.10:g.186292731GA[7], NG_023284.1:g.56717CT[5], NG_023284.1:g.56717CT[7]

Select item 149130107417.

rs1491301074 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 1:186327192 (GRCh38)
1:186296324 (GRCh37)
Canonical SPDI:: NC_000001.11:186327191:TT:
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000001.11:g.186327192_186327193del, NC_000001.10:g.186296324_186296325del, NG_023284.1:g.53133_53134del

Select item 149129681318.

rs1491296813 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT [Show Flanks]
Chromosome:: 1:186327274 (GRCh38)
1:186296406 (GRCh37)
Canonical SPDI:: NC_000001.11:186327272:TTT:T,NC_000001.11:186327272:TTT:TT,NC_000001.11:186327272:TTT:TTTT
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.00007/2 (TOMMO)
-=0.00242/4 (GnomAD)
HGVS:: NC_000001.11:g.186327274_186327275del, NC_000001.11:g.186327275del, NC_000001.11:g.186327275dup, NC_000001.10:g.186296406_186296407del, NC_000001.10:g.186296407del, NC_000001.10:g.186296407dup, NG_023284.1:g.53052_53053del, NG_023284.1:g.53053del, NG_023284.1:g.53053dup

Select item 149129365319.

rs1491293653 has merged into rs1216615267 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T [Show Flanks]
Chromosome:: 1:186327200 (GRCh38)
1:186296332 (GRCh37)
Canonical SPDI:: NC_000001.11:186327198:TTT:T,NC_000001.11:186327198:TTT:TT
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTT=0./0 (ALFA)
-=0.0002/5 (TOMMO)
HGVS:: NC_000001.11:g.186327200_186327201del, NC_000001.11:g.186327201del, NC_000001.10:g.186296332_186296333del, NC_000001.10:g.186296333del, NG_023284.1:g.53126_53127del, NG_023284.1:g.53127del

Select item 149125328320.

rs1491253283 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 1:186370168 (GRCh38)
1:186339300 (GRCh37)
Canonical SPDI:: NC_000001.11:186370167:CT:
Gene:: TPR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.186370168_186370169del, NC_000001.10:g.186339300_186339301del, NG_023284.1:g.10157_10158del

<< 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