rs267607897

Orientation

plus

Stabilized

plus

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

Make rs267607897(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37050605

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607897
dbSNP (classic)	rs267607897
ClinGen	rs267607897
ebi	rs267607897
HLI	rs267607897
Exac	rs267607897
Gnomad	rs267607897
Varsome	rs267607897
LitVar	rs267607897
Map	rs267607897
PheGenI	rs267607897
Biobank	rs267607897
1000 genomes	rs267607897
hgdp	rs267607897
ensembl	rs267607897
geneview	rs267607897
scholar	rs267607897
google	rs267607897
pharmgkb	rs267607897
gwascentral	rs267607897
openSNP	rs267607897
23andMe	rs267607897
SNPshot	rs267607897
SNPdbe	rs267607897
MSV3d	rs267607897
GWAS Ctlg	rs267607897

Max Magnitude

6

ClinVar
Risk	rs267607897(-;-)
Alt	rs267607897(-;-)
Reference	Rs267607897(GCAGCTTGCTA;GCAGCTTGCTA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37092096_37092106delGCAGCTTGCTA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075579.2,