rs587778922

Orientation

plus

Stabilized

plus

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

Make rs587778922(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

36996655

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778922
dbSNP (classic)	rs587778922
ClinGen	rs587778922
ebi	rs587778922
HLI	rs587778922
Exac	rs587778922
Gnomad	rs587778922
Varsome	rs587778922
LitVar	rs587778922
Map	rs587778922
PheGenI	rs587778922
Biobank	rs587778922
1000 genomes	rs587778922
hgdp	rs587778922
ensembl	rs587778922
geneview	rs587778922
scholar	rs587778922
google	rs587778922
pharmgkb	rs587778922
gwascentral	rs587778922
openSNP	rs587778922
23andMe	rs587778922
SNPshot	rs587778922
SNPdbe	rs587778922
MSV3d	rs587778922
GWAS Ctlg	rs587778922

Max Magnitude

6

ClinVar
Risk	rs587778922(T;T)
Alt	rs587778922(T;T)
Reference	Rs587778922(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038146dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075237.2,