Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852396

来自SNPedia
跳转至:导航搜索

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852396(A;T)
Make rs137852396(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154987242
GeneF8
is asnp
is mentioned by
dbSNPrs137852396
ebirs137852396
HLIrs137852396
Exacrs137852396
Varsomers137852396
Maprs137852396
PheGenIrs137852396
hapmaprs137852396
1000 genomesrs137852396
hgdprs137852396
ensemblrs137852396
gopubmedrs137852396
geneviewrs137852396
scholarrs137852396
googlers137852396
pharmgkbrs137852396
gwascentralrs137852396
openSNPrs137852396
23andMers137852396
23andMe allrs137852396
SNP Nexus

SNPshotrs137852396
SNPdbers137852396
MSV3drs137852396
GWAS Ctlgrs137852396
Max Magnitude0
OMIM306700
Desc
Variant0096
Relatedalso
ClinVar
Risk rs137852396(T;T)
Alt rs137852396(T;T)
Reference rs137852396(A;A)
Significance Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154215517T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010892.6,