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rs137852399

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852399(A;A)
Make rs137852399(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154969508
GeneF8
is asnp
is mentioned by
dbSNPrs137852399
ebirs137852399
HLIrs137852399
Exacrs137852399
Varsomers137852399
Maprs137852399
PheGenIrs137852399
hapmaprs137852399
1000 genomesrs137852399
hgdprs137852399
ensemblrs137852399
gopubmedrs137852399
geneviewrs137852399
scholarrs137852399
googlers137852399
pharmgkbrs137852399
gwascentralrs137852399
openSNPrs137852399
23andMers137852399
23andMe allrs137852399
SNP Nexus

SNPshotrs137852399
SNPdbers137852399
MSV3drs137852399
GWAS Ctlgrs137852399
Max Magnitude0
OMIM306700
Desc
Variant0104
Relatedalso
ClinVar
Risk rs137852399(A;A)
Alt rs137852399(A;A)
Reference rs137852399(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.154197783C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000010900.7,