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rs137852412

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs137852412(A;G)
Make rs137852412(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154961137
GeneF8
is asnp
is mentioned by
dbSNPrs137852412
ebirs137852412
HLIrs137852412
Exacrs137852412
Varsomers137852412
Maprs137852412
PheGenIrs137852412
hapmaprs137852412
1000 genomesrs137852412
hgdprs137852412
ensemblrs137852412
gopubmedrs137852412
geneviewrs137852412
scholarrs137852412
googlers137852412
pharmgkbrs137852412
gwascentralrs137852412
openSNPrs137852412
23andMers137852412
23andMe allrs137852412
SNP Nexus

SNPshotrs137852412
SNPdbers137852412
MSV3drs137852412
GWAS Ctlgrs137852412
Merged fromRs28937275
Max Magnitude0
OMIM306700
Desc
Variant0132
Relatedalso
ClinVar
Risk rs137852412(G;G)
Alt rs137852412(G;G)
Reference rs137852412(A;A)
Significance Probable-Pathogenic
Disease Hereditary factor VIII deficiency disease
Variation info
Gene F8
CLNDBN Hereditary factor VIII deficiency disease
Reversed 1
HGVS NC_000023.10:g.154189412T>C
CLNSRC
CLNACC