Have questions? Visit https://www.reddit.com/r/SNPedia

rs137852360

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852360(G;T)
Make rs137852360(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154837676
GeneF8
is asnp
is mentioned by
dbSNPrs137852360
ebirs137852360
HLIrs137852360
Exacrs137852360
Varsomers137852360
Maprs137852360
PheGenIrs137852360
hapmaprs137852360
1000 genomesrs137852360
hgdprs137852360
ensemblrs137852360
gopubmedrs137852360
geneviewrs137852360
scholarrs137852360
googlers137852360
pharmgkbrs137852360
gwascentralrs137852360
openSNPrs137852360
23andMers137852360
23andMe allrs137852360
SNP Nexus

SNPshotrs137852360
SNPdbers137852360
MSV3drs137852360
GWAS Ctlgrs137852360
Max Magnitude0
OMIM306700
Desc
Variant0025
Relatedalso
OMIM306700
Desc
Variant0042
Relatedalso
ClinVar
Risk rs137852360(A,T;A,T)
Alt rs137852360(A,T;A,T)
Reference rs137852360(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.154065951C>A; NC_000023.10:g.154065951C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010821.6, RCV000010839.6,