rs1060502888

Orientation

plus

Stabilized

plus

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

Make rs1060502888(-;-)

Make rs1060502888(-;CA)

Make rs1060502888(CA;CA)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47798856

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502888
dbSNP (classic)	rs1060502888
ClinGen	rs1060502888
ebi	rs1060502888
HLI	rs1060502888
Exac	rs1060502888
Gnomad	rs1060502888
Varsome	rs1060502888
LitVar	rs1060502888
Map	rs1060502888
PheGenI	rs1060502888
Biobank	rs1060502888
1000 genomes	rs1060502888
hgdp	rs1060502888
ensembl	rs1060502888
geneview	rs1060502888
scholar	rs1060502888
google	rs1060502888
pharmgkb	rs1060502888
gwascentral	rs1060502888
openSNP	rs1060502888
23andMe	rs1060502888
SNPshot	rs1060502888
SNPdbe	rs1060502888
MSV3d	rs1060502888
GWAS Ctlg	rs1060502888

Max Magnitude

0

ClinVar
Risk	rs1060502888(-;-)
Alt	rs1060502888(-;-)
Reference	Rs1060502888(AC;AC)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48025995_48025996delCA
CLNSRC
CLNACC	RCV000473969.1,