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rs137852370

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs137852370(C;C)
Make rs137852370(C;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966655
GeneF8
is asnp
is mentioned by
dbSNPrs137852370
ebirs137852370
HLIrs137852370
Exacrs137852370
Varsomers137852370
Maprs137852370
PheGenIrs137852370
hapmaprs137852370
1000 genomesrs137852370
hgdprs137852370
ensemblrs137852370
gopubmedrs137852370
geneviewrs137852370
scholarrs137852370
googlers137852370
pharmgkbrs137852370
gwascentralrs137852370
openSNPrs137852370
23andMers137852370
23andMe allrs137852370
SNP Nexus

SNPshotrs137852370
SNPdbers137852370
MSV3drs137852370
GWAS Ctlgrs137852370
Max Magnitude0
OMIM306700
Desc
Variant0058
Relatedalso
ClinVar
Risk rs137852370(C;C)
Alt rs137852370(C;C)
Reference rs137852370(T;T)
Significance Probable-Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154194930A>G
CLNSRC
CLNACC