rs786203924

Orientation

plus

Stabilized

plus

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

Make rs786203924(-;-)

Make rs786203924(-;AT)

Make rs786203924(AT;AT)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47800889

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs786203924
dbSNP (classic)	rs786203924
ClinGen	rs786203924
ebi	rs786203924
HLI	rs786203924
Exac	rs786203924
Gnomad	rs786203924
Varsome	rs786203924
LitVar	rs786203924
Map	rs786203924
PheGenI	rs786203924
Biobank	rs786203924
1000 genomes	rs786203924
hgdp	rs786203924
ensembl	rs786203924
geneview	rs786203924
scholar	rs786203924
google	rs786203924
pharmgkb	rs786203924
gwascentral	rs786203924
openSNP	rs786203924
23andMe	rs786203924
SNPshot	rs786203924
SNPdbe	rs786203924
MSV3d	rs786203924
GWAS Ctlg	rs786203924

Max Magnitude

0

ClinVar
Risk	rs786203924(-;-)
Alt	rs786203924(-;-)
Reference	Rs786203924(TA;TA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48028028_48028029delAT
CLNSRC
CLNACC	RCV000167441.2,