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

rs137852434

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852434(C;C)
Make rs137852434(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154947782
GeneF8
is asnp
is mentioned by
dbSNPrs137852434
ebirs137852434
HLIrs137852434
Exacrs137852434
Varsomers137852434
Maprs137852434
PheGenIrs137852434
hapmaprs137852434
1000 genomesrs137852434
hgdprs137852434
ensemblrs137852434
gopubmedrs137852434
geneviewrs137852434
scholarrs137852434
googlers137852434
pharmgkbrs137852434
gwascentralrs137852434
openSNPrs137852434
23andMers137852434
23andMe allrs137852434
SNP Nexus

SNPshotrs137852434
SNPdbers137852434
MSV3drs137852434
GWAS Ctlgrs137852434
Max Magnitude0
OMIM306700
Desc
Variant0161
Relatedalso
ClinVar
Risk rs137852434(C;C)
Alt rs137852434(C;C)
Reference rs137852434(T;T)
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.154176057A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010957.3,