rs193922374

Orientation

plus

Stabilized

plus

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

Make rs193922374(A;G)

Make rs193922374(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410148

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs193922374
dbSNP (classic)	rs193922374
ClinGen	rs193922374
ebi	rs193922374
HLI	rs193922374
Exac	rs193922374
Gnomad	rs193922374
Varsome	rs193922374
LitVar	rs193922374
Map	rs193922374
PheGenI	rs193922374
Biobank	rs193922374
1000 genomes	rs193922374
hgdp	rs193922374
ensembl	rs193922374
geneview	rs193922374
scholar	rs193922374
google	rs193922374
pharmgkb	rs193922374
gwascentral	rs193922374
openSNP	rs193922374
23andMe	rs193922374
SNPshot	rs193922374
SNPdbe	rs193922374
MSV3d	rs193922374
GWAS Ctlg	rs193922374

Max Magnitude

0

ClinVar
Risk	rs193922374(G;G)
Alt	rs193922374(G;G)
Reference	Rs193922374(A;A)
Significance	Probable-Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000002.11:g.47637287A>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000030254.3, RCV000115531.6, RCV000212584.1,