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rs137852430

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852430(C;C)
Make rs137852430(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154947853
GeneF8
is asnp
is mentioned by
dbSNPrs137852430
ebirs137852430
HLIrs137852430
Exacrs137852430
Varsomers137852430
Maprs137852430
PheGenIrs137852430
hapmaprs137852430
1000 genomesrs137852430
hgdprs137852430
ensemblrs137852430
gopubmedrs137852430
geneviewrs137852430
scholarrs137852430
googlers137852430
pharmgkbrs137852430
gwascentralrs137852430
openSNPrs137852430
23andMers137852430
23andMe allrs137852430
SNP Nexus

SNPshotrs137852430
SNPdbers137852430
MSV3drs137852430
GWAS Ctlgrs137852430
Max Magnitude0
OMIM306700
Desc
Variant0156
Relatedalso
ClinVar
Risk rs137852430(C;C)
Alt rs137852430(C;C)
Reference rs137852430(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.154176128A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010952.4,