rs63750735

Orientation

plus

Stabilized

plus

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

Make rs63750735(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47799789

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750735
dbSNP (classic)	rs63750735
ClinGen	rs63750735
ebi	rs63750735
HLI	rs63750735
Exac	rs63750735
Gnomad	rs63750735
Varsome	rs63750735
LitVar	rs63750735
Map	rs63750735
PheGenI	rs63750735
Biobank	rs63750735
1000 genomes	rs63750735
hgdp	rs63750735
ensembl	rs63750735
geneview	rs63750735
scholar	rs63750735
google	rs63750735
pharmgkb	rs63750735
gwascentral	rs63750735
openSNP	rs63750735
23andMe	rs63750735
SNPshot	rs63750735
SNPdbe	rs63750735
MSV3d	rs63750735
GWAS Ctlg	rs63750735

Max Magnitude

6

c.1806_1809delAAAG (p.Glu604Leufs)

23andMe name: i5037872

ClinVar
Risk	rs63750735(-;-)
Alt	rs63750735(-;-)
Reference	Rs63750735(AAAG;AAAG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48026928_48026931delAAAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074687.2,