rs63751469

Orientation

plus

Stabilized

plus

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

Make rs63751469(A;A)

Make rs63751469(A;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47482779

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751469
dbSNP (classic)	rs63751469
ClinGen	rs63751469
ebi	rs63751469
HLI	rs63751469
Exac	rs63751469
Gnomad	rs63751469
Varsome	rs63751469
LitVar	rs63751469
Map	rs63751469
PheGenI	rs63751469
Biobank	rs63751469
1000 genomes	rs63751469
hgdp	rs63751469
ensembl	rs63751469
geneview	rs63751469
scholar	rs63751469
google	rs63751469
pharmgkb	rs63751469
gwascentral	rs63751469
openSNP	rs63751469
23andMe	rs63751469
SNPshot	rs63751469
SNPdbe	rs63751469
MSV3d	rs63751469
GWAS Ctlg	rs63751469

Max Magnitude

0

ClinVar
Risk	rs63751469(A;A) rs63751469(T;T)
Alt	rs63751469(A;A) rs63751469(T;T)
Reference	Rs63751469(C;C)
Significance	Pathogenic
Disease	Lynch syndrome I Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome I Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47709918C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076530.2, RCV000491055.1,