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

rs137852256

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852256(G;T)
Make rs137852256(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position139561749
GeneF9
is asnp
is mentioned by
dbSNPrs137852256
ebirs137852256
HLIrs137852256
Exacrs137852256
Varsomers137852256
Maprs137852256
PheGenIrs137852256
hapmaprs137852256
1000 genomesrs137852256
hgdprs137852256
ensemblrs137852256
gopubmedrs137852256
geneviewrs137852256
scholarrs137852256
googlers137852256
pharmgkbrs137852256
gwascentralrs137852256
openSNPrs137852256
23andMers137852256
23andMe allrs137852256
SNP Nexus

SNPshotrs137852256
SNPdbers137852256
MSV3drs137852256
GWAS Ctlgrs137852256
Max Magnitude0
OMIM300746
Desc
Variant0052
Relatedalso
ClinVar
Risk rs137852256(T;T)
Alt rs137852256(T;T)
Reference rs137852256(G;G)
Significance Pathogenic
Disease Hereditary factor IX deficiency disease
Variation info
Gene F9
CLNDBN Hereditary factor IX deficiency disease
Reversed 0
HGVS NC_000023.10:g.138643908G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000011355.1,