rs63751118

Orientation

plus

Stabilized

plus

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

Make rs63751118(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025850

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751118
dbSNP (classic)	rs63751118
ClinGen	rs63751118
ebi	rs63751118
HLI	rs63751118
Exac	rs63751118
Gnomad	rs63751118
Varsome	rs63751118
LitVar	rs63751118
Map	rs63751118
PheGenI	rs63751118
Biobank	rs63751118
1000 genomes	rs63751118
hgdp	rs63751118
ensembl	rs63751118
geneview	rs63751118
scholar	rs63751118
google	rs63751118
pharmgkb	rs63751118
gwascentral	rs63751118
openSNP	rs63751118
23andMe	rs63751118
SNPshot	rs63751118
SNPdbe	rs63751118
MSV3d	rs63751118
GWAS Ctlg	rs63751118

Max Magnitude

6

ClinVar
Risk	rs63751118(-;-)
Alt	rs63751118(-;-)
Reference	Rs63751118(AG;AG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067341_37067342delGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075159.2,