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rs137852400

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852400(G;G)
Make rs137852400(G;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154969486
GeneF8
is asnp
is mentioned by
dbSNPrs137852400
ebirs137852400
HLIrs137852400
Exacrs137852400
Varsomers137852400
Maprs137852400
PheGenIrs137852400
hapmaprs137852400
1000 genomesrs137852400
hgdprs137852400
ensemblrs137852400
gopubmedrs137852400
geneviewrs137852400
scholarrs137852400
googlers137852400
pharmgkbrs137852400
gwascentralrs137852400
openSNPrs137852400
23andMers137852400
23andMe allrs137852400
SNP Nexus

SNPshotrs137852400
SNPdbers137852400
MSV3drs137852400
GWAS Ctlgrs137852400
Max Magnitude0
OMIM306700
Desc
Variant0106
Relatedalso
ClinVar
Risk rs137852400(G;G)
Alt rs137852400(G;G)
Reference rs137852400(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.154197761A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000010902.4,