rs121909243

Orientation

plus

Stabilized

plus

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

Make rs121909243(A;T)

Make rs121909243(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

12416923

Gene

PPARG

is a	snp
is	mentioned by
dbSNP	rs121909243
dbSNP (classic)	rs121909243
ClinGen	rs121909243
ebi	rs121909243
HLI	rs121909243
Exac	rs121909243
Gnomad	rs121909243
Varsome	rs121909243
LitVar	rs121909243
Map	rs121909243
PheGenI	rs121909243
Biobank	rs121909243
1000 genomes	rs121909243
hgdp	rs121909243
ensembl	rs121909243
geneview	rs121909243
scholar	rs121909243
google	rs121909243
pharmgkb	rs121909243
gwascentral	rs121909243
openSNP	rs121909243
23andMe	rs121909243
SNPshot	rs121909243
SNPdbe	rs121909243
MSV3d	rs121909243
GWAS Ctlg	rs121909243

Max Magnitude

0

OMIM	601487
Desc
Variant	0005
Related	also

ClinVar
Risk	rs121909243(T;T)
Alt	rs121909243(T;T)
Reference	Rs121909243(A;A)
Significance	Pathogenic
Disease	Carcinoma of colon
Variation	info
Gene	PPARG
CLNDBN	Carcinoma of colon
Reversed	0
HGVS	NC_000003.11:g.12458422A>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000008610.4,