rs587778930

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;TTC)	6	Lynch syndrome, pathogenic mutation
(CTT;CTT)	0	common in clinvar
(TTC;TTC)	0	common/normal

Make rs587778930(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37040215

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778930
dbSNP (classic)	rs587778930
ClinGen	rs587778930
ebi	rs587778930
HLI	rs587778930
Exac	rs587778930
Gnomad	rs587778930
Varsome	rs587778930
LitVar	rs587778930
Map	rs587778930
PheGenI	rs587778930
Biobank	rs587778930
1000 genomes	rs587778930
hgdp	rs587778930
ensembl	rs587778930
geneview	rs587778930
scholar	rs587778930
google	rs587778930
pharmgkb	rs587778930
gwascentral	rs587778930
openSNP	rs587778930
23andMe	rs587778930
SNPshot	rs587778930
SNPdbe	rs587778930
MSV3d	rs587778930
GWAS Ctlg	rs587778930

Max Magnitude

6

ClinVar
Risk	rs587778930(-;-)
Alt	rs587778930(-;-)
Reference	Rs587778930(CTT;CTT)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000003.11:g.37081706_37081708delTTC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075272.2, RCV000130099.2,