rs587779019

Orientation

plus

Stabilized

plus

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

Make rs587779019(GA;GA)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37008884

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779019
dbSNP (classic)	rs587779019
ClinGen	rs587779019
ebi	rs587779019
HLI	rs587779019
Exac	rs587779019
Gnomad	rs587779019
Varsome	rs587779019
LitVar	rs587779019
Map	rs587779019
PheGenI	rs587779019
Biobank	rs587779019
1000 genomes	rs587779019
hgdp	rs587779019
ensembl	rs587779019
geneview	rs587779019
scholar	rs587779019
google	rs587779019
pharmgkb	rs587779019
gwascentral	rs587779019
openSNP	rs587779019
23andMe	rs587779019
SNPshot	rs587779019
SNPdbe	rs587779019
MSV3d	rs587779019
GWAS Ctlg	rs587779019

Max Magnitude

6

ClinVar
Risk	rs587779019(AG;AG) rs587779019(GA;GA)
Alt	rs587779019(AG;AG) rs587779019(GA;GA)
Reference	Rs587779019(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37050375_37050376insGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075742.2,