rs63750741

Orientation

plus

Stabilized

plus

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

Make rs63750741(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799329

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750741
dbSNP (classic)	rs63750741
ClinGen	rs63750741
ebi	rs63750741
HLI	rs63750741
Exac	rs63750741
Gnomad	rs63750741
Varsome	rs63750741
LitVar	rs63750741
Map	rs63750741
PheGenI	rs63750741
Biobank	rs63750741
1000 genomes	rs63750741
hgdp	rs63750741
ensembl	rs63750741
geneview	rs63750741
scholar	rs63750741
google	rs63750741
pharmgkb	rs63750741
gwascentral	rs63750741
openSNP	rs63750741
23andMe	rs63750741
SNPshot	rs63750741
SNPdbe	rs63750741
MSV3d	rs63750741
GWAS Ctlg	rs63750741

Max Magnitude

6

ClinVar
Risk	rs63750741(C;C)
Alt	rs63750741(C;C)
Reference	Rs63750741(T;T)
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.48026468T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000074651.2, RCV000491070.1,