rs182024561

Orientation

plus

Stabilized

plus

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

Make rs182024561(C;T)

Make rs182024561(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47805662

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs182024561
dbSNP (classic)	rs182024561
ClinGen	rs182024561
ebi	rs182024561
HLI	rs182024561
Exac	rs182024561
Gnomad	rs182024561
Varsome	rs182024561
LitVar	rs182024561
Map	rs182024561
PheGenI	rs182024561
Biobank	rs182024561
1000 genomes	rs182024561
hgdp	rs182024561
ensembl	rs182024561
geneview	rs182024561
scholar	rs182024561
google	rs182024561
pharmgkb	rs182024561
gwascentral	rs182024561
openSNP	rs182024561
23andMe	rs182024561
SNPshot	rs182024561
SNPdbe	rs182024561
MSV3d	rs182024561
GWAS Ctlg	rs182024561

Max Magnitude

0

ClinVar
Risk	rs182024561(G;G) rs182024561(T;T)
Alt	rs182024561(G;G) rs182024561(T;T)
Reference	Rs182024561(C;C)
Significance	Probable-Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000002.11:g.48032801C>G; NC_000002.11:g.48032801C>T
CLNSRC
CLNACC	RCV000074891.2, RCV000220560.2, RCV000483164.1, RCV000220632.1,