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rs137852398

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852398(A;A)
Make rs137852398(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154969543
GeneF8
is asnp
is mentioned by
dbSNPrs137852398
ebirs137852398
HLIrs137852398
Exacrs137852398
Varsomers137852398
Maprs137852398
PheGenIrs137852398
hapmaprs137852398
1000 genomesrs137852398
hgdprs137852398
ensemblrs137852398
gopubmedrs137852398
geneviewrs137852398
scholarrs137852398
googlers137852398
pharmgkbrs137852398
gwascentralrs137852398
openSNPrs137852398
23andMers137852398
23andMe allrs137852398
SNP Nexus

SNPshotrs137852398
SNPdbers137852398
MSV3drs137852398
GWAS Ctlgrs137852398
Max Magnitude0
OMIM306700
Desc
Variant0102
Relatedalso
ClinVar
Risk rs137852398(A;A)
Alt rs137852398(A;A)
Reference rs137852398(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.154197818C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010898.3,