rs63750466

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs63750466(A;A)

Make rs63750466(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403195

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750466
dbSNP (classic)	rs63750466
ClinGen	rs63750466
ebi	rs63750466
HLI	rs63750466
Exac	rs63750466
Gnomad	rs63750466
Varsome	rs63750466
LitVar	rs63750466
Map	rs63750466
PheGenI	rs63750466
Biobank	rs63750466
1000 genomes	rs63750466
hgdp	rs63750466
ensembl	rs63750466
geneview	rs63750466
scholar	rs63750466
google	rs63750466
pharmgkb	rs63750466
gwascentral	rs63750466
openSNP	rs63750466
23andMe	rs63750466
SNPshot	rs63750466
SNPdbe	rs63750466
MSV3d	rs63750466
GWAS Ctlg	rs63750466

Max Magnitude

0

ClinVar
Risk	rs63750466(A;A)
Alt	rs63750466(A;A)
Reference	Rs63750466(G;G)
Significance	Probable-non-pathogenic
Disease	not provided Lynch syndrome I Hereditary cancer-predisposing syndrome not specified Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	not provided Lynch syndrome I Hereditary cancer-predisposing syndrome not specified Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47630334G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000034558.1, RCV000076617.3, RCV000115534.7, RCV000202071.2, RCV000206355.3,