rs1060500698

Orientation

plus

Stabilized

plus

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

Make rs1060500698(-;-)

Make rs1060500698(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

3

Position

37050641

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs1060500698
dbSNP (classic)	rs1060500698
ClinGen	rs1060500698
ebi	rs1060500698
HLI	rs1060500698
Exac	rs1060500698
Gnomad	rs1060500698
Varsome	rs1060500698
LitVar	rs1060500698
Map	rs1060500698
PheGenI	rs1060500698
Biobank	rs1060500698
1000 genomes	rs1060500698
hgdp	rs1060500698
ensembl	rs1060500698
geneview	rs1060500698
scholar	rs1060500698
google	rs1060500698
pharmgkb	rs1060500698
gwascentral	rs1060500698
openSNP	rs1060500698
23andMe	rs1060500698
SNPshot	rs1060500698
SNPdbe	rs1060500698
MSV3d	rs1060500698
GWAS Ctlg	rs1060500698

Max Magnitude

0

ClinVar
Risk	rs1060500698(-;-)
Alt	rs1060500698(-;-)
Reference	Rs1060500698(T;T)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37092132delT
CLNSRC
CLNACC	RCV000463125.1,