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rs137852461

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852461(A;A)
Make rs137852461(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154863151
GeneF8
is asnp
is mentioned by
dbSNPrs137852461
ebirs137852461
HLIrs137852461
Exacrs137852461
Varsomers137852461
Maprs137852461
PheGenIrs137852461
hapmaprs137852461
1000 genomesrs137852461
hgdprs137852461
ensemblrs137852461
gopubmedrs137852461
geneviewrs137852461
scholarrs137852461
googlers137852461
pharmgkbrs137852461
gwascentralrs137852461
openSNPrs137852461
23andMers137852461
23andMe allrs137852461
SNP Nexus

SNPshotrs137852461
SNPdbers137852461
MSV3drs137852461
GWAS Ctlgrs137852461
Max Magnitude0
OMIM306700
Desc
Variant0231
Relatedalso
ClinVar
Risk rs137852461(A;A)
Alt rs137852461(A;A)
Reference rs137852461(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.154091426C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011028.7,