rs63751453

Orientation

plus

Stabilized

plus

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

Make rs63751453(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476496

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751453
dbSNP (classic)	rs63751453
ClinGen	rs63751453
ebi	rs63751453
HLI	rs63751453
Exac	rs63751453
Gnomad	rs63751453
Varsome	rs63751453
LitVar	rs63751453
Map	rs63751453
PheGenI	rs63751453
Biobank	rs63751453
1000 genomes	rs63751453
hgdp	rs63751453
ensembl	rs63751453
geneview	rs63751453
scholar	rs63751453
google	rs63751453
pharmgkb	rs63751453
gwascentral	rs63751453
openSNP	rs63751453
23andMe	rs63751453
SNPshot	rs63751453
SNPdbe	rs63751453
MSV3d	rs63751453
GWAS Ctlg	rs63751453

Max Magnitude

6

ClinVar
Risk	rs63751453(T;T)
Alt	rs63751453(T;T)
Reference	Rs63751453(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703635dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076406.2,