rs786204144

Orientation

plus

Stabilized

plus

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

Make rs786204144(-;A)

Make rs786204144(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47412550

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786204144
dbSNP (classic)	rs786204144
ClinGen	rs786204144
ebi	rs786204144
HLI	rs786204144
Exac	rs786204144
Gnomad	rs786204144
Varsome	rs786204144
LitVar	rs786204144
Map	rs786204144
PheGenI	rs786204144
Biobank	rs786204144
1000 genomes	rs786204144
hgdp	rs786204144
ensembl	rs786204144
geneview	rs786204144
scholar	rs786204144
google	rs786204144
pharmgkb	rs786204144
gwascentral	rs786204144
openSNP	rs786204144
23andMe	rs786204144
SNPshot	rs786204144
SNPdbe	rs786204144
MSV3d	rs786204144
GWAS Ctlg	rs786204144

Max Magnitude

0

ClinVar
Risk	rs786204144(A;A)
Alt	rs786204144(A;A)
Reference	Rs786204144(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639689_47639690insA
CLNSRC
CLNACC	RCV000168130.1,