rs63749981

Orientation

plus

Stabilized

plus

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

Make rs63749981(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025941

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749981
dbSNP (classic)	rs63749981
ClinGen	rs63749981
ebi	rs63749981
HLI	rs63749981
Exac	rs63749981
Gnomad	rs63749981
Varsome	rs63749981
LitVar	rs63749981
Map	rs63749981
PheGenI	rs63749981
Biobank	rs63749981
1000 genomes	rs63749981
hgdp	rs63749981
ensembl	rs63749981
geneview	rs63749981
scholar	rs63749981
google	rs63749981
pharmgkb	rs63749981
gwascentral	rs63749981
openSNP	rs63749981
23andMe	rs63749981
SNPshot	rs63749981
SNPdbe	rs63749981
MSV3d	rs63749981
GWAS Ctlg	rs63749981

Max Magnitude

6

ClinVar
Risk	rs63749981(-;-)
Alt	rs63749981(-;-)
Reference	Rs63749981(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067432delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075175.2,