rs63749945

Orientation

plus

Stabilized

plus

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

Make rs63749945(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47416326

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749945
dbSNP (classic)	rs63749945
ClinGen	rs63749945
ebi	rs63749945
HLI	rs63749945
Exac	rs63749945
Gnomad	rs63749945
Varsome	rs63749945
LitVar	rs63749945
Map	rs63749945
PheGenI	rs63749945
Biobank	rs63749945
1000 genomes	rs63749945
hgdp	rs63749945
ensembl	rs63749945
geneview	rs63749945
scholar	rs63749945
google	rs63749945
pharmgkb	rs63749945
gwascentral	rs63749945
openSNP	rs63749945
23andMe	rs63749945
SNPshot	rs63749945
SNPdbe	rs63749945
MSV3d	rs63749945
GWAS Ctlg	rs63749945

Max Magnitude

6

ClinVar
Risk	rs63749945(T;T)
Alt	rs63749945(T;T)
Reference	Rs63749945(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47643465dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076771.2,