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

rs137852421

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852421(G;T)
Make rs137852421(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154956983
GeneF8
is asnp
is mentioned by
dbSNPrs137852421
ebirs137852421
HLIrs137852421
Exacrs137852421
Varsomers137852421
Maprs137852421
PheGenIrs137852421
hapmaprs137852421
1000 genomesrs137852421
hgdprs137852421
ensemblrs137852421
gopubmedrs137852421
geneviewrs137852421
scholarrs137852421
googlers137852421
pharmgkbrs137852421
gwascentralrs137852421
openSNPrs137852421
23andMers137852421
23andMe allrs137852421
SNP Nexus

SNPshotrs137852421
SNPdbers137852421
MSV3drs137852421
GWAS Ctlgrs137852421
Max Magnitude0
OMIM306700
Desc
Variant0145
Relatedalso
ClinVar
Risk rs137852421(T;T)
Alt rs137852421(T;T)
Reference rs137852421(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.154185258C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000010941.5,