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rs137852449

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852449(A;A)
Make rs137852449(A;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position154904022
GeneF8
is asnp
is mentioned by
dbSNPrs137852449
ebirs137852449
HLIrs137852449
Exacrs137852449
Varsomers137852449
Maprs137852449
PheGenIrs137852449
hapmaprs137852449
1000 genomesrs137852449
hgdprs137852449
ensemblrs137852449
gopubmedrs137852449
geneviewrs137852449
scholarrs137852449
googlers137852449
pharmgkbrs137852449
gwascentralrs137852449
openSNPrs137852449
23andMers137852449
23andMe allrs137852449
SNP Nexus

SNPshotrs137852449
SNPdbers137852449
MSV3drs137852449
GWAS Ctlgrs137852449
Max Magnitude0
OMIM306700
Desc
Variant0213
Relatedalso
ClinVar
Risk rs137852449(A;A)
Alt rs137852449(A;A)
Reference rs137852449(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.154132297C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011009.6,