rs267607729

Orientation

plus

Stabilized

plus

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

Make rs267607729(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37000991

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607729
dbSNP (classic)	rs267607729
ClinGen	rs267607729
ebi	rs267607729
HLI	rs267607729
Exac	rs267607729
Gnomad	rs267607729
Varsome	rs267607729
LitVar	rs267607729
Map	rs267607729
PheGenI	rs267607729
Biobank	rs267607729
1000 genomes	rs267607729
hgdp	rs267607729
ensembl	rs267607729
geneview	rs267607729
scholar	rs267607729
google	rs267607729
pharmgkb	rs267607729
gwascentral	rs267607729
openSNP	rs267607729
23andMe	rs267607729
SNPshot	rs267607729
SNPdbe	rs267607729
MSV3d	rs267607729
GWAS Ctlg	rs267607729

Max Magnitude

6

ClinVar
Risk	rs267607729(A;A)
Alt	rs267607729(A;A)
Reference	Rs267607729(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37042482dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075603.2,