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rs137852429

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852429(A;G)
Make rs137852429(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154953903
GeneF8
is asnp
is mentioned by
dbSNPrs137852429
ebirs137852429
HLIrs137852429
Exacrs137852429
Varsomers137852429
Maprs137852429
PheGenIrs137852429
hapmaprs137852429
1000 genomesrs137852429
hgdprs137852429
ensemblrs137852429
gopubmedrs137852429
geneviewrs137852429
scholarrs137852429
googlers137852429
pharmgkbrs137852429
gwascentralrs137852429
openSNPrs137852429
23andMers137852429
23andMe allrs137852429
SNP Nexus

SNPshotrs137852429
SNPdbers137852429
MSV3drs137852429
GWAS Ctlgrs137852429
Max Magnitude0
OMIM306700
Desc
Variant0154
Relatedalso
ClinVar
Risk rs137852429(G;G)
Alt rs137852429(G;G)
Reference rs137852429(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.154182178T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010950.5,