rs63750996

Orientation

plus

Stabilized

plus

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

Make rs63750996(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47798689

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750996
dbSNP (classic)	rs63750996
ClinGen	rs63750996
ebi	rs63750996
HLI	rs63750996
Exac	rs63750996
Gnomad	rs63750996
Varsome	rs63750996
LitVar	rs63750996
Map	rs63750996
PheGenI	rs63750996
Biobank	rs63750996
1000 genomes	rs63750996
hgdp	rs63750996
ensembl	rs63750996
geneview	rs63750996
scholar	rs63750996
google	rs63750996
pharmgkb	rs63750996
gwascentral	rs63750996
openSNP	rs63750996
23andMe	rs63750996
SNPshot	rs63750996
SNPdbe	rs63750996
MSV3d	rs63750996
GWAS Ctlg	rs63750996

Max Magnitude

6

ClinVar
Risk	rs63750996(T;T)
Alt	rs63750996(T;T)
Reference	Rs63750996(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48025828C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075026.2,