rs63749845

Orientation

plus

Stabilized

plus

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

Make rs63749845(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025932

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749845
dbSNP (classic)	rs63749845
ClinGen	rs63749845
ebi	rs63749845
HLI	rs63749845
Exac	rs63749845
Gnomad	rs63749845
Varsome	rs63749845
LitVar	rs63749845
Map	rs63749845
PheGenI	rs63749845
Biobank	rs63749845
1000 genomes	rs63749845
hgdp	rs63749845
ensembl	rs63749845
geneview	rs63749845
scholar	rs63749845
google	rs63749845
pharmgkb	rs63749845
gwascentral	rs63749845
openSNP	rs63749845
23andMe	rs63749845
SNPshot	rs63749845
SNPdbe	rs63749845
MSV3d	rs63749845
GWAS Ctlg	rs63749845

Max Magnitude

6

ClinVar
Risk	rs63749845(-;-)
Alt	rs63749845(-;-)
Reference	Rs63749845(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067423delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075173.2,