rs63750845

Orientation

plus

Stabilized

plus

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

Make rs63750845(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47466734

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750845
dbSNP (classic)	rs63750845
ClinGen	rs63750845
ebi	rs63750845
HLI	rs63750845
Exac	rs63750845
Gnomad	rs63750845
Varsome	rs63750845
LitVar	rs63750845
Map	rs63750845
PheGenI	rs63750845
Biobank	rs63750845
1000 genomes	rs63750845
hgdp	rs63750845
ensembl	rs63750845
geneview	rs63750845
scholar	rs63750845
google	rs63750845
pharmgkb	rs63750845
gwascentral	rs63750845
openSNP	rs63750845
23andMe	rs63750845
SNPshot	rs63750845
SNPdbe	rs63750845
MSV3d	rs63750845
GWAS Ctlg	rs63750845

Max Magnitude

6

ClinVar
Risk	rs63750845(-;-)
Alt	rs63750845(-;-)
Reference	Rs63750845(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47693873delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076201.2,