rs63750904

Orientation

plus

Stabilized

plus

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

Make rs63750904(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47800702

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs63750904
dbSNP (classic)	rs63750904
ClinGen	rs63750904
ebi	rs63750904
HLI	rs63750904
Exac	rs63750904
Gnomad	rs63750904
Varsome	rs63750904
LitVar	rs63750904
Map	rs63750904
PheGenI	rs63750904
Biobank	rs63750904
1000 genomes	rs63750904
hgdp	rs63750904
ensembl	rs63750904
geneview	rs63750904
scholar	rs63750904
google	rs63750904
pharmgkb	rs63750904
gwascentral	rs63750904
openSNP	rs63750904
23andMe	rs63750904
SNPshot	rs63750904
SNPdbe	rs63750904
MSV3d	rs63750904
GWAS Ctlg	rs63750904

Max Magnitude

6

ClinVar
Risk	rs63750904(-;-)
Alt	rs63750904(-;-)
Reference	Rs63750904(TG;TG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027841_48027842delGT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074776.2,