rs587779048

Orientation

plus

Stabilized

plus

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

Make rs587779048(AC;AC)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

37017582

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587779048
dbSNP (classic)	rs587779048
ClinGen	rs587779048
ebi	rs587779048
HLI	rs587779048
Exac	rs587779048
Gnomad	rs587779048
Varsome	rs587779048
LitVar	rs587779048
Map	rs587779048
PheGenI	rs587779048
Biobank	rs587779048
1000 genomes	rs587779048
hgdp	rs587779048
ensembl	rs587779048
geneview	rs587779048
scholar	rs587779048
google	rs587779048
pharmgkb	rs587779048
gwascentral	rs587779048
openSNP	rs587779048
23andMe	rs587779048
SNPshot	rs587779048
SNPdbe	rs587779048
MSV3d	rs587779048
GWAS Ctlg	rs587779048

Max Magnitude

6

ClinVar
Risk	rs587779048(AC;AC)
Alt	rs587779048(AC;AC)
Reference	Rs587779048(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37059072_37059073dupAC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075895.2,