rs63751614

Orientation

plus

Stabilized

plus

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

Make rs63751614(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47412556

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751614
dbSNP (classic)	rs63751614
ClinGen	rs63751614
ebi	rs63751614
HLI	rs63751614
Exac	rs63751614
Gnomad	rs63751614
Varsome	rs63751614
LitVar	rs63751614
Map	rs63751614
PheGenI	rs63751614
Biobank	rs63751614
1000 genomes	rs63751614
hgdp	rs63751614
ensembl	rs63751614
geneview	rs63751614
scholar	rs63751614
google	rs63751614
pharmgkb	rs63751614
gwascentral	rs63751614
openSNP	rs63751614
23andMe	rs63751614
SNPshot	rs63751614
SNPdbe	rs63751614
MSV3d	rs63751614
GWAS Ctlg	rs63751614

Max Magnitude

6

ClinVar
Risk	rs63751614(-;-)
Alt	rs63751614(-;-)
Reference	Rs63751614(AT;AT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639695_47639696delAT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076708.2,