rs63750377

Orientation

plus

Stabilized

plus

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

Make rs63750377(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47803567

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750377
dbSNP (classic)	rs63750377
ClinGen	rs63750377
ebi	rs63750377
HLI	rs63750377
Exac	rs63750377
Gnomad	rs63750377
Varsome	rs63750377
LitVar	rs63750377
Map	rs63750377
PheGenI	rs63750377
Biobank	rs63750377
1000 genomes	rs63750377
hgdp	rs63750377
ensembl	rs63750377
geneview	rs63750377
scholar	rs63750377
google	rs63750377
pharmgkb	rs63750377
gwascentral	rs63750377
openSNP	rs63750377
23andMe	rs63750377
SNPshot	rs63750377
SNPdbe	rs63750377
MSV3d	rs63750377
GWAS Ctlg	rs63750377

Max Magnitude

6

ClinVar
Risk	rs63750377(-;-)
Alt	rs63750377(-;-)
Reference	Rs63750377(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48030706delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074839.2,