rs6691847

Orientation

plus

Stabilized

plus

Make rs6691847(C;C)

Make rs6691847(C;T)

Make rs6691847(T;T)

Reference

GRCh38 38.1/141

Chromosome

1

Position

29792805

is a	snp
is	mentioned by
dbSNP	rs6691847
dbSNP (classic)	rs6691847
ClinGen	rs6691847
ebi	rs6691847
HLI	rs6691847
Exac	rs6691847
Gnomad	rs6691847
Varsome	rs6691847
LitVar	rs6691847
Map	rs6691847
PheGenI	rs6691847
Biobank	rs6691847
1000 genomes	rs6691847
hgdp	rs6691847
ensembl	rs6691847
geneview	rs6691847
scholar	rs6691847
google	rs6691847
pharmgkb	rs6691847
gwascentral	rs6691847
openSNP	rs6691847
23andMe	rs6691847
SNPshot	rs6691847
SNPdbe	rs6691847
MSV3d	rs6691847
GWAS Ctlg	rs6691847

GMAF

0.1818

Max Magnitude

0

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

GWAS snp
PMID	[PMID 23535911]
Trait	Non-alcoholic fatty liver disease
Title	Genome-wide scan revealed that polymorphisms in the PNPLA3, SAMM50, and PARVB genes are associated with development and progression of nonalcoholic fatty liver disease in Japan.
Risk Allele	C
P-val	7E-6
Odds Ratio	1.32 [0.98-1.77]