rs267607734

Orientation

plus

Stabilized

plus

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

Make rs267607734(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37001054

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs267607734
dbSNP (classic)	rs267607734
ClinGen	rs267607734
ebi	rs267607734
HLI	rs267607734
Exac	rs267607734
Gnomad	rs267607734
Varsome	rs267607734
LitVar	rs267607734
Map	rs267607734
PheGenI	rs267607734
Biobank	rs267607734
1000 genomes	rs267607734
hgdp	rs267607734
ensembl	rs267607734
geneview	rs267607734
scholar	rs267607734
google	rs267607734
pharmgkb	rs267607734
gwascentral	rs267607734
openSNP	rs267607734
23andMe	rs267607734
SNPshot	rs267607734
SNPdbe	rs267607734
MSV3d	rs267607734
GWAS Ctlg	rs267607734

Max Magnitude

6

ClinVar
Risk	rs267607734(A;A)
Alt	rs267607734(A;A)
Reference	Rs267607734(G;G)
Significance	Pathogenic
Disease	Lynch syndrome I
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome I
Reversed	0
HGVS	NC_000003.11:g.37042545G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075628.3,