rs587778923

Orientation

plus

Stabilized

plus

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

Make rs587778923(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

3

Position

36996657

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs587778923
dbSNP (classic)	rs587778923
ClinGen	rs587778923
ebi	rs587778923
HLI	rs587778923
Exac	rs587778923
Gnomad	rs587778923
Varsome	rs587778923
LitVar	rs587778923
Map	rs587778923
PheGenI	rs587778923
Biobank	rs587778923
1000 genomes	rs587778923
hgdp	rs587778923
ensembl	rs587778923
geneview	rs587778923
scholar	rs587778923
google	rs587778923
pharmgkb	rs587778923
gwascentral	rs587778923
openSNP	rs587778923
23andMe	rs587778923
SNPshot	rs587778923
SNPdbe	rs587778923
MSV3d	rs587778923
GWAS Ctlg	rs587778923

Max Magnitude

6

ClinVar
Risk	rs587778923(-;-) Rs587778923(AAAG;AAAG)
Alt	rs587778923(-;-) Rs587778923(AAAG;AAAG)
Reference	Rs587778923(AAGA;AAGA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038148_37038151delAAGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075264.2,