rs878853702

Orientation

plus

Stabilized

plus

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

Make rs878853702(-;-)

Make rs878853702(-;AT)

Make rs878853702(AT;AT)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47799333

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs878853702
dbSNP (classic)	rs878853702
ClinGen	rs878853702
ebi	rs878853702
HLI	rs878853702
Exac	rs878853702
Gnomad	rs878853702
Varsome	rs878853702
LitVar	rs878853702
Map	rs878853702
PheGenI	rs878853702
Biobank	rs878853702
1000 genomes	rs878853702
hgdp	rs878853702
ensembl	rs878853702
geneview	rs878853702
scholar	rs878853702
google	rs878853702
pharmgkb	rs878853702
gwascentral	rs878853702
openSNP	rs878853702
23andMe	rs878853702
SNPshot	rs878853702
SNPdbe	rs878853702
MSV3d	rs878853702
GWAS Ctlg	rs878853702

Max Magnitude

0

ClinVar
Risk	rs878853702(-;-)
Alt	rs878853702(-;-)
Reference	Rs878853702(TA;TA)
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.48026472_48026473delAT
CLNSRC
CLNACC	RCV000228751.1, RCV000491947.1,