rs63749926

Orientation

plus

Stabilized

plus

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

Make rs63749926(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37020379

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749926
dbSNP (classic)	rs63749926
ClinGen	rs63749926
ebi	rs63749926
HLI	rs63749926
Exac	rs63749926
Gnomad	rs63749926
Varsome	rs63749926
LitVar	rs63749926
Map	rs63749926
PheGenI	rs63749926
Biobank	rs63749926
1000 genomes	rs63749926
hgdp	rs63749926
ensembl	rs63749926
geneview	rs63749926
scholar	rs63749926
google	rs63749926
pharmgkb	rs63749926
gwascentral	rs63749926
openSNP	rs63749926
23andMe	rs63749926
SNPshot	rs63749926
SNPdbe	rs63749926
MSV3d	rs63749926
GWAS Ctlg	rs63749926

Max Magnitude

6

ClinVar
Risk	rs63749926(-;-)
Alt	rs63749926(-;-)
Reference	Rs63749926(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37061870delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075944.2,