rs10108954

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics

Make rs10108954(C;T)

Make rs10108954(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

8864868

Gene

MFHAS1

is a	snp
is	mentioned by
dbSNP	rs10108954
dbSNP (classic)	rs10108954
ClinGen	rs10108954
ebi	rs10108954
HLI	rs10108954
Exac	rs10108954
Gnomad	rs10108954
Varsome	rs10108954
LitVar	rs10108954
Map	rs10108954
PheGenI	rs10108954
Biobank	rs10108954
1000 genomes	rs10108954
hgdp	rs10108954
ensembl	rs10108954
geneview	rs10108954
scholar	rs10108954
google	rs10108954
pharmgkb	rs10108954
gwascentral	rs10108954
openSNP	rs10108954
23andMe	rs10108954
SNPshot	rs10108954
SNPdbe	rs10108954
MSV3d	rs10108954
GWAS Ctlg	rs10108954

GMAF

0.1143

Max Magnitude

0

?	(C;C) (C;T) (T;T)	28

GWAS snp
PMID	[PMID 22210626]
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