rs193922375

Orientation

plus

Stabilized

plus

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

Make rs193922375(-;G)

Make rs193922375(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414336

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs193922375
dbSNP (classic)	rs193922375
ClinGen	rs193922375
ebi	rs193922375
HLI	rs193922375
Exac	rs193922375
Gnomad	rs193922375
Varsome	rs193922375
LitVar	rs193922375
Map	rs193922375
PheGenI	rs193922375
Biobank	rs193922375
1000 genomes	rs193922375
hgdp	rs193922375
ensembl	rs193922375
geneview	rs193922375
scholar	rs193922375
google	rs193922375
pharmgkb	rs193922375
gwascentral	rs193922375
openSNP	rs193922375
23andMe	rs193922375
SNPshot	rs193922375
SNPdbe	rs193922375
MSV3d	rs193922375
GWAS Ctlg	rs193922375

Max Magnitude

0

ClinVar
Risk	rs193922375(G;G)
Alt	rs193922375(G;G)
Reference	Rs193922375(-;-)
Significance	Other
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47641475dupG
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030255.2, RCV000162420.2,