rs587776687

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs587776687(-;-)

Make rs587776687(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

12392689

Gene

PPARG

is a	snp
is	mentioned by
dbSNP	rs587776687
dbSNP (classic)	rs587776687
ClinGen	rs587776687
ebi	rs587776687
HLI	rs587776687
Exac	rs587776687
Gnomad	rs587776687
Varsome	rs587776687
LitVar	rs587776687
Map	rs587776687
PheGenI	rs587776687
Biobank	rs587776687
1000 genomes	rs587776687
hgdp	rs587776687
ensembl	rs587776687
geneview	rs587776687
scholar	rs587776687
google	rs587776687
pharmgkb	rs587776687
gwascentral	rs587776687
openSNP	rs587776687
23andMe	rs587776687
SNPshot	rs587776687
SNPdbe	rs587776687
MSV3d	rs587776687
GWAS Ctlg	rs587776687

Max Magnitude

0

ClinVar
Risk	rs587776687(-;-)
Alt	rs587776687(-;-)
Reference	Rs587776687(A;A)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	PPARG
CLNDBN	Carcinoma of colon
Reversed	0
HGVS	NC_000003.11:g.12434188delA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008608.4,