rs63750086

Orientation

plus

Stabilized

plus

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

Make rs63750086(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429891

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750086
dbSNP (classic)	rs63750086
ClinGen	rs63750086
ebi	rs63750086
HLI	rs63750086
Exac	rs63750086
Gnomad	rs63750086
Varsome	rs63750086
LitVar	rs63750086
Map	rs63750086
PheGenI	rs63750086
Biobank	rs63750086
1000 genomes	rs63750086
hgdp	rs63750086
ensembl	rs63750086
geneview	rs63750086
scholar	rs63750086
google	rs63750086
pharmgkb	rs63750086
gwascentral	rs63750086
openSNP	rs63750086
23andMe	rs63750086
SNPshot	rs63750086
SNPdbe	rs63750086
MSV3d	rs63750086
GWAS Ctlg	rs63750086

Max Magnitude

6

ClinVar
Risk	rs63750086(-;-)
Alt	rs63750086(-;-)
Reference	Rs63750086(AG;AG)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided Lynch syndrome I
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided Lynch syndrome I
Reversed	0
HGVS	NC_000002.11:g.47657030_47657031delAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076073.2, RCV000160629.4, RCV000212600.2, RCV000411649.1,