rs63750618

Orientation

plus

Stabilized

plus

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

Make rs63750618(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478395

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750618
dbSNP (classic)	rs63750618
ClinGen	rs63750618
ebi	rs63750618
HLI	rs63750618
Exac	rs63750618
Gnomad	rs63750618
Varsome	rs63750618
LitVar	rs63750618
Map	rs63750618
PheGenI	rs63750618
Biobank	rs63750618
1000 genomes	rs63750618
hgdp	rs63750618
ensembl	rs63750618
geneview	rs63750618
scholar	rs63750618
google	rs63750618
pharmgkb	rs63750618
gwascentral	rs63750618
openSNP	rs63750618
23andMe	rs63750618
SNPshot	rs63750618
SNPdbe	rs63750618
MSV3d	rs63750618
GWAS Ctlg	rs63750618

Max Magnitude

6

ClinVar
Risk	rs63750618(A;A)
Alt	rs63750618(A;A)
Reference	Rs63750618(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47705534C>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076458.2, RCV000115517.3, RCV000491112.1,