rs121918714

Orientation

plus

Stabilized

plus

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

Make rs121918714(C;C)

Make rs121918714(C;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

30691471

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs121918714
dbSNP (classic)	rs121918714
ClinGen	rs121918714
ebi	rs121918714
HLI	rs121918714
Exac	rs121918714
Gnomad	rs121918714
Varsome	rs121918714
LitVar	rs121918714
Map	rs121918714
PheGenI	rs121918714
Biobank	rs121918714
1000 genomes	rs121918714
hgdp	rs121918714
ensembl	rs121918714
geneview	rs121918714
scholar	rs121918714
google	rs121918714
pharmgkb	rs121918714
gwascentral	rs121918714
openSNP	rs121918714
23andMe	rs121918714
SNPshot	rs121918714
SNPdbe	rs121918714
MSV3d	rs121918714
GWAS Ctlg	rs121918714

Max Magnitude

0

OMIM	190182
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918714(C;C)
Alt	rs121918714(C;C)
Reference	Rs121918714(G;G)
Significance	Pathogenic
Disease	Malignant tumor of esophagus
Variation	info
Gene	TGFBR2
CLNDBN	Malignant tumor of esophagus
Reversed	0
HGVS	NC_000003.11:g.30732963G>C
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000013326.5,