rs63750564

Orientation

plus

Stabilized

plus

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

Make rs63750564(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799818

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750564
dbSNP (classic)	rs63750564
ClinGen	rs63750564
ebi	rs63750564
HLI	rs63750564
Exac	rs63750564
Gnomad	rs63750564
Varsome	rs63750564
LitVar	rs63750564
Map	rs63750564
PheGenI	rs63750564
Biobank	rs63750564
1000 genomes	rs63750564
hgdp	rs63750564
ensembl	rs63750564
geneview	rs63750564
scholar	rs63750564
google	rs63750564
pharmgkb	rs63750564
gwascentral	rs63750564
openSNP	rs63750564
23andMe	rs63750564
SNPshot	rs63750564
SNPdbe	rs63750564
MSV3d	rs63750564
GWAS Ctlg	rs63750564

Max Magnitude

6

ClinVar
Risk	rs63750564(A;A)
Alt	rs63750564(A;A)
Reference	Rs63750564(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48026957C>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074690.2,