rs587778947

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;T)	6	Lynch syndrome, pathogenic mutation

Make rs587778947(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37047608

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778947
dbSNP (classic)	rs587778947
ClinGen	rs587778947
ebi	rs587778947
HLI	rs587778947
Exac	rs587778947
Gnomad	rs587778947
Varsome	rs587778947
LitVar	rs587778947
Map	rs587778947
PheGenI	rs587778947
Biobank	rs587778947
1000 genomes	rs587778947
hgdp	rs587778947
ensembl	rs587778947
geneview	rs587778947
scholar	rs587778947
google	rs587778947
pharmgkb	rs587778947
gwascentral	rs587778947
openSNP	rs587778947
23andMe	rs587778947
SNPshot	rs587778947
SNPdbe	rs587778947
MSV3d	rs587778947
GWAS Ctlg	rs587778947

Max Magnitude

6

ClinVar
Risk	rs587778947(T;T)
Alt	rs587778947(T;T)
Reference	Rs587778947(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089099dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075373.2,