rs1060502881

Orientation

plus

Stabilized

plus

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

Make rs1060502881(-;-)

Make rs1060502881(-;GAATT)

Make rs1060502881(GAATT;GAATT)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47805638

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502881
dbSNP (classic)	rs1060502881
ClinGen	rs1060502881
ebi	rs1060502881
HLI	rs1060502881
Exac	rs1060502881
Gnomad	rs1060502881
Varsome	rs1060502881
LitVar	rs1060502881
Map	rs1060502881
PheGenI	rs1060502881
Biobank	rs1060502881
1000 genomes	rs1060502881
hgdp	rs1060502881
ensembl	rs1060502881
geneview	rs1060502881
scholar	rs1060502881
google	rs1060502881
pharmgkb	rs1060502881
gwascentral	rs1060502881
openSNP	rs1060502881
23andMe	rs1060502881
SNPshot	rs1060502881
SNPdbe	rs1060502881
MSV3d	rs1060502881
GWAS Ctlg	rs1060502881

Max Magnitude

0

ClinVar
Risk	rs1060502881(-;-)
Alt	rs1060502881(-;-)
Reference	Rs1060502881(TTGAA;TTGAA)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48032777_48032781delGAATT
CLNSRC
CLNACC	RCV000465518.1, RCV000482445.1,