rs63749930

Orientation

plus

Stabilized

plus

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

Make rs63749930(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47466699

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749930
dbSNP (classic)	rs63749930
ClinGen	rs63749930
ebi	rs63749930
HLI	rs63749930
Exac	rs63749930
Gnomad	rs63749930
Varsome	rs63749930
LitVar	rs63749930
Map	rs63749930
PheGenI	rs63749930
Biobank	rs63749930
1000 genomes	rs63749930
hgdp	rs63749930
ensembl	rs63749930
geneview	rs63749930
scholar	rs63749930
google	rs63749930
pharmgkb	rs63749930
gwascentral	rs63749930
openSNP	rs63749930
23andMe	rs63749930
SNPshot	rs63749930
SNPdbe	rs63749930
MSV3d	rs63749930
GWAS Ctlg	rs63749930

Max Magnitude

6

ClinVar
Risk	rs63749930(-;-)
Alt	rs63749930(-;-)
Reference	Rs63749930(CA;CA)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47693838_47693839delCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076193.2, RCV000235817.1,