rs878853711

Orientation

plus

Stabilized

plus

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

Make rs878853711(CTTCTACCTCAAAAA;CTTCTACCTCAAAAA)

Make rs878853711(CTTCTACCTCAAAAA;GGTTG)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47800039

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs878853711
dbSNP (classic)	rs878853711
ClinGen	rs878853711
ebi	rs878853711
HLI	rs878853711
Exac	rs878853711
Gnomad	rs878853711
Varsome	rs878853711
LitVar	rs878853711
Map	rs878853711
PheGenI	rs878853711
Biobank	rs878853711
1000 genomes	rs878853711
hgdp	rs878853711
ensembl	rs878853711
geneview	rs878853711
scholar	rs878853711
google	rs878853711
pharmgkb	rs878853711
gwascentral	rs878853711
openSNP	rs878853711
23andMe	rs878853711
SNPshot	rs878853711
SNPdbe	rs878853711
MSV3d	rs878853711
GWAS Ctlg	rs878853711

Max Magnitude

0

ClinVar
Risk	rs878853711(CTTCTACCTCAAAAA;CTTCTACCTCAAAAA)
Alt	rs878853711(CTTCTACCTCAAAAA;CTTCTACCTCAAAAA)
Reference	Rs878853711(GGTTG;GGTTG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027178_48027182delGGTTGinsCTTCTACCTCAAAAA
CLNSRC
CLNACC	RCV000226342.2,