rs541623924

Orientation

plus

Stabilized

plus

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

Make rs541623924(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47475272

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs541623924
dbSNP (classic)	rs541623924
ClinGen	rs541623924
ebi	rs541623924
HLI	rs541623924
Exac	rs541623924
Gnomad	rs541623924
Varsome	rs541623924
LitVar	rs541623924
Map	rs541623924
PheGenI	rs541623924
Biobank	rs541623924
1000 genomes	rs541623924
hgdp	rs541623924
ensembl	rs541623924
geneview	rs541623924
scholar	rs541623924
google	rs541623924
pharmgkb	rs541623924
gwascentral	rs541623924
openSNP	rs541623924
23andMe	rs541623924
SNPshot	rs541623924
SNPdbe	rs541623924
MSV3d	rs541623924
GWAS Ctlg	rs541623924

Max Magnitude

0

ClinVar
Risk	rs541623924(A;A) Rs541623924(T;T)
Alt	rs541623924(A;A) Rs541623924(T;T)
Reference	Rs541623924(-;-)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47702411dup; NC_000002.11:g.47702411dupT
CLNSRC
CLNACC	RCV000491289.1, RCV000202039.1,