rs786204257

Orientation

plus

Stabilized

plus

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

Make rs786204257(-;T)

Make rs786204257(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47408450

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786204257
dbSNP (classic)	rs786204257
ClinGen	rs786204257
ebi	rs786204257
HLI	rs786204257
Exac	rs786204257
Gnomad	rs786204257
Varsome	rs786204257
LitVar	rs786204257
Map	rs786204257
PheGenI	rs786204257
Biobank	rs786204257
1000 genomes	rs786204257
hgdp	rs786204257
ensembl	rs786204257
geneview	rs786204257
scholar	rs786204257
google	rs786204257
pharmgkb	rs786204257
gwascentral	rs786204257
openSNP	rs786204257
23andMe	rs786204257
SNPshot	rs786204257
SNPdbe	rs786204257
MSV3d	rs786204257
GWAS Ctlg	rs786204257

Max Magnitude

0

ClinVar
Risk	rs786204257(T;T)
Alt	rs786204257(T;T)
Reference	Rs786204257(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635589dupT
CLNSRC
CLNACC	RCV000168462.1,