rs786202193

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TTTTTTGATGACAG)	6	Lynch syndrome
(ACAGTTTTTTGATG;ACAGTTTTTTGATG)	0	common in clinvar
(TTTTTTGATGACAG;TTTTTTGATGACAG)	0	common/normal

Make rs786202193(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47791063

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs786202193
dbSNP (classic)	rs786202193
ClinGen	rs786202193
ebi	rs786202193
HLI	rs786202193
Exac	rs786202193
Gnomad	rs786202193
Varsome	rs786202193
LitVar	rs786202193
Map	rs786202193
PheGenI	rs786202193
Biobank	rs786202193
1000 genomes	rs786202193
hgdp	rs786202193
ensembl	rs786202193
geneview	rs786202193
scholar	rs786202193
google	rs786202193
pharmgkb	rs786202193
gwascentral	rs786202193
openSNP	rs786202193
23andMe	rs786202193
SNPshot	rs786202193
SNPdbe	rs786202193
MSV3d	rs786202193
GWAS Ctlg	rs786202193

Max Magnitude

6

ClinVar
Risk	rs786202193(-;-)
Alt	rs786202193(-;-)
Reference	Rs786202193(ACAGTTTTTTGATG;ACAGTTTTTTGATG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48018202_48018215delTTTTTTGATGACAG
CLNSRC
CLNACC	RCV000164894.1,