rs863224829

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AGTA;AGTA)	0	common in clinvar

Make rs863224829(-;-)

Make rs863224829(-;AGTA)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47799593

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs863224829
dbSNP (classic)	rs863224829
ClinGen	rs863224829
ebi	rs863224829
HLI	rs863224829
Exac	rs863224829
Gnomad	rs863224829
Varsome	rs863224829
LitVar	rs863224829
Map	rs863224829
PheGenI	rs863224829
Biobank	rs863224829
1000 genomes	rs863224829
hgdp	rs863224829
ensembl	rs863224829
geneview	rs863224829
scholar	rs863224829
google	rs863224829
pharmgkb	rs863224829
gwascentral	rs863224829
openSNP	rs863224829
23andMe	rs863224829
SNPshot	rs863224829
SNPdbe	rs863224829
MSV3d	rs863224829
GWAS Ctlg	rs863224829

Merged from

Rs771764652

Max Magnitude

0

ClinVar
Risk	rs863224829(-;-)
Alt	rs863224829(-;-)
Reference	Rs863224829(AGTA;AGTA)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48026732_48026735delAGTA
CLNSRC
CLNACC	RCV000196707.1, RCV000213843.2,