rs63751602

Orientation

plus

Stabilized

plus

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

Make rs63751602(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47412418

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751602
dbSNP (classic)	rs63751602
ClinGen	rs63751602
ebi	rs63751602
HLI	rs63751602
Exac	rs63751602
Gnomad	rs63751602
Varsome	rs63751602
LitVar	rs63751602
Map	rs63751602
PheGenI	rs63751602
Biobank	rs63751602
1000 genomes	rs63751602
hgdp	rs63751602
ensembl	rs63751602
geneview	rs63751602
scholar	rs63751602
google	rs63751602
pharmgkb	rs63751602
gwascentral	rs63751602
openSNP	rs63751602
23andMe	rs63751602
SNPshot	rs63751602
SNPdbe	rs63751602
MSV3d	rs63751602
GWAS Ctlg	rs63751602

Max Magnitude

6

ClinVar
Risk	rs63751602(-;-)
Alt	rs63751602(-;-)
Reference	Rs63751602(AATTC;AATTC)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47639557_47639561delTTCAA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076676.2, RCV000492017.1,