rs63751027

Orientation

plus

Stabilized

plus

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

Make rs63751027(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47416387

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751027
dbSNP (classic)	rs63751027
ClinGen	rs63751027
ebi	rs63751027
HLI	rs63751027
Exac	rs63751027
Gnomad	rs63751027
Varsome	rs63751027
LitVar	rs63751027
Map	rs63751027
PheGenI	rs63751027
Biobank	rs63751027
1000 genomes	rs63751027
hgdp	rs63751027
ensembl	rs63751027
geneview	rs63751027
scholar	rs63751027
google	rs63751027
pharmgkb	rs63751027
gwascentral	rs63751027
openSNP	rs63751027
23andMe	rs63751027
SNPshot	rs63751027
SNPdbe	rs63751027
MSV3d	rs63751027
GWAS Ctlg	rs63751027

Max Magnitude

6

ClinVar
Risk	rs63751027(A;A)
Alt	rs63751027(A;A)
Reference	Rs63751027(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47643526G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076004.2,