rs1060500689

Orientation

plus

Stabilized

plus

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

Make rs1060500689(C;G)

Make rs1060500689(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

37007000

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs1060500689
dbSNP (classic)	rs1060500689
ClinGen	rs1060500689
ebi	rs1060500689
HLI	rs1060500689
Exac	rs1060500689
Gnomad	rs1060500689
Varsome	rs1060500689
LitVar	rs1060500689
Map	rs1060500689
PheGenI	rs1060500689
Biobank	rs1060500689
1000 genomes	rs1060500689
hgdp	rs1060500689
ensembl	rs1060500689
geneview	rs1060500689
scholar	rs1060500689
google	rs1060500689
pharmgkb	rs1060500689
gwascentral	rs1060500689
openSNP	rs1060500689
23andMe	rs1060500689
SNPshot	rs1060500689
SNPdbe	rs1060500689
MSV3d	rs1060500689
GWAS Ctlg	rs1060500689

Max Magnitude

0

ClinVar
Risk	rs1060500689(G;G)
Alt	rs1060500689(G;G)
Reference	Rs1060500689(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37048491C>G
CLNSRC
CLNACC	RCV000470067.1,