rs587776769

Orientation

plus

Stabilized

plus

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

Make rs587776769(-;TG)

Make rs587776769(TG;TG)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

30691497

Gene

TGFBR2

is a	snp
is	mentioned by
dbSNP	rs587776769
dbSNP (classic)	rs587776769
ClinGen	rs587776769
ebi	rs587776769
HLI	rs587776769
Exac	rs587776769
Gnomad	rs587776769
Varsome	rs587776769
LitVar	rs587776769
Map	rs587776769
PheGenI	rs587776769
Biobank	rs587776769
1000 genomes	rs587776769
hgdp	rs587776769
ensembl	rs587776769
geneview	rs587776769
scholar	rs587776769
google	rs587776769
pharmgkb	rs587776769
gwascentral	rs587776769
openSNP	rs587776769
23andMe	rs587776769
SNPshot	rs587776769
SNPdbe	rs587776769
MSV3d	rs587776769
GWAS Ctlg	rs587776769

Max Magnitude

0

ClinVar
Risk	rs587776769(GT;GT)
Alt	rs587776769(GT;GT)
Reference	Rs587776769(-;-)
Significance	Pathogenic
Disease	Hereditary nonpolyposis colorectal cancer type 6
Variation	info
Gene	TGFBR2
CLNDBN	Hereditary nonpolyposis colorectal cancer type 6
Reversed	0
HGVS	NC_000003.11:g.30732988_30732989dupTG
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013324.4,