rs121909242

Orientation

plus

Stabilized

plus

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

Make rs121909242(A;C)

Make rs121909242(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12416825

Gene

PPARG

is a	snp
is	mentioned by
dbSNP	rs121909242
dbSNP (classic)	rs121909242
ClinGen	rs121909242
ebi	rs121909242
HLI	rs121909242
Exac	rs121909242
Gnomad	rs121909242
Varsome	rs121909242
LitVar	rs121909242
Map	rs121909242
PheGenI	rs121909242
Biobank	rs121909242
1000 genomes	rs121909242
hgdp	rs121909242
ensembl	rs121909242
geneview	rs121909242
scholar	rs121909242
google	rs121909242
pharmgkb	rs121909242
gwascentral	rs121909242
openSNP	rs121909242
23andMe	rs121909242
SNPshot	rs121909242
SNPdbe	rs121909242
MSV3d	rs121909242
GWAS Ctlg	rs121909242

Max Magnitude

0

OMIM	601487
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121909242(C;C)
Alt	rs121909242(C;C)
Reference	Rs121909242(A;A)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	PPARG
CLNDBN	Carcinoma of colon
Reversed	0
HGVS	NC_000003.11:g.12458324A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008609.4,