rs63750552

Orientation

plus

Stabilized

plus

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

Make rs63750552(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47798797

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750552
dbSNP (classic)	rs63750552
ClinGen	rs63750552
ebi	rs63750552
HLI	rs63750552
Exac	rs63750552
Gnomad	rs63750552
Varsome	rs63750552
LitVar	rs63750552
Map	rs63750552
PheGenI	rs63750552
Biobank	rs63750552
1000 genomes	rs63750552
hgdp	rs63750552
ensembl	rs63750552
geneview	rs63750552
scholar	rs63750552
google	rs63750552
pharmgkb	rs63750552
gwascentral	rs63750552
openSNP	rs63750552
23andMe	rs63750552
SNPshot	rs63750552
SNPdbe	rs63750552
MSV3d	rs63750552
GWAS Ctlg	rs63750552

Max Magnitude

6

ClinVar
Risk	rs63750552(T;T)
Alt	rs63750552(T;T)
Reference	Rs63750552(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48025936G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075038.2,