rs63750408

Orientation

plus

Stabilized

plus

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

Make rs63750408(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410135

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750408
dbSNP (classic)	rs63750408
ClinGen	rs63750408
ebi	rs63750408
HLI	rs63750408
Exac	rs63750408
Gnomad	rs63750408
Varsome	rs63750408
LitVar	rs63750408
Map	rs63750408
PheGenI	rs63750408
Biobank	rs63750408
1000 genomes	rs63750408
hgdp	rs63750408
ensembl	rs63750408
geneview	rs63750408
scholar	rs63750408
google	rs63750408
pharmgkb	rs63750408
gwascentral	rs63750408
openSNP	rs63750408
23andMe	rs63750408
SNPshot	rs63750408
SNPdbe	rs63750408
MSV3d	rs63750408
GWAS Ctlg	rs63750408

Merged from

Rs776948651

Max Magnitude

6

ClinVar
Risk	rs63750408(-;-)
Alt	rs63750408(-;-)
Reference	Rs63750408(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637274delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076596.2,