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rs137852410

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852410(C;C)
Make rs137852410(C;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154966654
GeneF8
is asnp
is mentioned by
dbSNPrs137852410
ebirs137852410
HLIrs137852410
Exacrs137852410
Varsomers137852410
Maprs137852410
PheGenIrs137852410
hapmaprs137852410
1000 genomesrs137852410
hgdprs137852410
ensemblrs137852410
gopubmedrs137852410
geneviewrs137852410
scholarrs137852410
googlers137852410
pharmgkbrs137852410
gwascentralrs137852410
openSNPrs137852410
23andMers137852410
23andMe allrs137852410
SNP Nexus

SNPshotrs137852410
SNPdbers137852410
MSV3drs137852410
GWAS Ctlgrs137852410
Max Magnitude0
OMIM306700
Desc
Variant0119
Relatedalso
ClinVar
Risk rs137852410(C;C)
Alt rs137852410(C;C)
Reference rs137852410(G;G)
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.154194929C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000010915.6,