rs63751435

Orientation

plus

Stabilized

plus

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

Make rs63751435(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37028865

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751435
dbSNP (classic)	rs63751435
ClinGen	rs63751435
ebi	rs63751435
HLI	rs63751435
Exac	rs63751435
Gnomad	rs63751435
Varsome	rs63751435
LitVar	rs63751435
Map	rs63751435
PheGenI	rs63751435
Biobank	rs63751435
1000 genomes	rs63751435
hgdp	rs63751435
ensembl	rs63751435
geneview	rs63751435
scholar	rs63751435
google	rs63751435
pharmgkb	rs63751435
gwascentral	rs63751435
openSNP	rs63751435
23andMe	rs63751435
SNPshot	rs63751435
SNPdbe	rs63751435
MSV3d	rs63751435
GWAS Ctlg	rs63751435

Max Magnitude

6

ClinVar
Risk	rs63751435(-;-)
Alt	rs63751435(-;-)
Reference	Rs63751435(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37070356delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075228.2,