rs878853709

Orientation

plus

Stabilized

plus

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

Make rs878853709(-;C)

Make rs878853709(C;C)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47799553

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs878853709
dbSNP (classic)	rs878853709
ClinGen	rs878853709
ebi	rs878853709
HLI	rs878853709
Exac	rs878853709
Gnomad	rs878853709
Varsome	rs878853709
LitVar	rs878853709
Map	rs878853709
PheGenI	rs878853709
Biobank	rs878853709
1000 genomes	rs878853709
hgdp	rs878853709
ensembl	rs878853709
geneview	rs878853709
scholar	rs878853709
google	rs878853709
pharmgkb	rs878853709
gwascentral	rs878853709
openSNP	rs878853709
23andMe	rs878853709
SNPshot	rs878853709
SNPdbe	rs878853709
MSV3d	rs878853709
GWAS Ctlg	rs878853709

Max Magnitude

0

ClinVar
Risk	rs878853709(C;C)
Alt	rs878853709(C;C)
Reference	Rs878853709(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48026692_48026693insC
CLNSRC
CLNACC	RCV000231145.1,