rs587779012

Orientation

plus

Stabilized

plus

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

Make rs587779012(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37006999

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779012
dbSNP (classic)	rs587779012
ClinGen	rs587779012
ebi	rs587779012
HLI	rs587779012
Exac	rs587779012
Gnomad	rs587779012
Varsome	rs587779012
LitVar	rs587779012
Map	rs587779012
PheGenI	rs587779012
Biobank	rs587779012
1000 genomes	rs587779012
hgdp	rs587779012
ensembl	rs587779012
geneview	rs587779012
scholar	rs587779012
google	rs587779012
pharmgkb	rs587779012
gwascentral	rs587779012
openSNP	rs587779012
23andMe	rs587779012
SNPshot	rs587779012
SNPdbe	rs587779012
MSV3d	rs587779012
GWAS Ctlg	rs587779012

Max Magnitude

6

ClinVar
Risk	rs587779012(-;-)
Alt	rs587779012(-;-)
Reference	Rs587779012(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37048490delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075694.2,