rs267607881

Orientation

plus

Stabilized

plus

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

Make rs267607881(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048888

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607881
dbSNP (classic)	rs267607881
ClinGen	rs267607881
ebi	rs267607881
HLI	rs267607881
Exac	rs267607881
Gnomad	rs267607881
Varsome	rs267607881
LitVar	rs267607881
Map	rs267607881
PheGenI	rs267607881
Biobank	rs267607881
1000 genomes	rs267607881
hgdp	rs267607881
ensembl	rs267607881
geneview	rs267607881
scholar	rs267607881
google	rs267607881
pharmgkb	rs267607881
gwascentral	rs267607881
openSNP	rs267607881
23andMe	rs267607881
SNPshot	rs267607881
SNPdbe	rs267607881
MSV3d	rs267607881
GWAS Ctlg	rs267607881

Max Magnitude

6

ClinVar
Risk	rs267607881(-;-)
Alt	rs267607881(-;-)
Reference	Rs267607881(AATTTCTTTGGACCA;AATTTCTTTGGACCA)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090379_37090393delAATTTCTTTGGACCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075466.2,