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rs10108954

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10108954(C;T)
Make rs10108954(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position8864868
GeneMFHAS1
is asnp
is mentioned by
dbSNPrs10108954
ebirs10108954
HLIrs10108954
Exacrs10108954
Varsomers10108954
Maprs10108954
PheGenIrs10108954
hapmaprs10108954
1000 genomesrs10108954
hgdprs10108954
ensemblrs10108954
gopubmedrs10108954
geneviewrs10108954
scholarrs10108954
googlers10108954
pharmgkbrs10108954
gwascentralrs10108954
openSNPrs10108954
23andMers10108954
23andMe allrs10108954
SNP Nexus

SNPshotrs10108954
SNPdbers10108954
MSV3drs10108954
GWAS Ctlgrs10108954
GMAF0.1143
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22210626OA-icon.png]
Trait
Title Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Risk Allele
P-val 0.000007
Odds Ratio 1.7359 None