rs63750111

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;C)	6	Lynch syndrome
(C;C)	0	common in clinvar
(C;G)	6	Lynch syndrome, pathogenic mutation

Make rs63750111(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47800914

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750111
dbSNP (classic)	rs63750111
ClinGen	rs63750111
ebi	rs63750111
HLI	rs63750111
Exac	rs63750111
Gnomad	rs63750111
Varsome	rs63750111
LitVar	rs63750111
Map	rs63750111
PheGenI	rs63750111
Biobank	rs63750111
1000 genomes	rs63750111
hgdp	rs63750111
ensembl	rs63750111
geneview	rs63750111
scholar	rs63750111
google	rs63750111
pharmgkb	rs63750111
gwascentral	rs63750111
openSNP	rs63750111
23andMe	rs63750111
SNPshot	rs63750111
SNPdbe	rs63750111
MSV3d	rs63750111
GWAS Ctlg	rs63750111

Max Magnitude

6

ClinVar
Risk	rs63750111(G;G)
Alt	rs63750111(G;G)
Reference	Rs63750111(C;C)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48028053C>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074788.2, RCV000491868.1,