rs63751015

Orientation

plus

Stabilized

plus

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

Make rs63751015(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025808

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751015
dbSNP (classic)	rs63751015
ClinGen	rs63751015
ebi	rs63751015
HLI	rs63751015
Exac	rs63751015
Gnomad	rs63751015
Varsome	rs63751015
LitVar	rs63751015
Map	rs63751015
PheGenI	rs63751015
Biobank	rs63751015
1000 genomes	rs63751015
hgdp	rs63751015
ensembl	rs63751015
geneview	rs63751015
scholar	rs63751015
google	rs63751015
pharmgkb	rs63751015
gwascentral	rs63751015
openSNP	rs63751015
23andMe	rs63751015
SNPshot	rs63751015
SNPdbe	rs63751015
MSV3d	rs63751015
GWAS Ctlg	rs63751015

Max Magnitude

6

ClinVar
Risk	rs63751015(-;-)
Alt	rs63751015(-;-)
Reference	Rs63751015(CT;CT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067299_37067300delCT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075150.2,