rs63750140

Orientation

plus

Stabilized

plus

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

Make rs63750140(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47800798

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750140
dbSNP (classic)	rs63750140
ClinGen	rs63750140
ebi	rs63750140
HLI	rs63750140
Exac	rs63750140
Gnomad	rs63750140
Varsome	rs63750140
LitVar	rs63750140
Map	rs63750140
PheGenI	rs63750140
Biobank	rs63750140
1000 genomes	rs63750140
hgdp	rs63750140
ensembl	rs63750140
geneview	rs63750140
scholar	rs63750140
google	rs63750140
pharmgkb	rs63750140
gwascentral	rs63750140
openSNP	rs63750140
23andMe	rs63750140
SNPshot	rs63750140
SNPdbe	rs63750140
MSV3d	rs63750140
GWAS Ctlg	rs63750140

Max Magnitude

6

ClinVar
Risk	rs63750140(T;T)
Alt	rs63750140(T;T)
Reference	Rs63750140(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.48027937C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074783.2, RCV000491935.1,