rs63751653

Orientation

plus

Stabilized

plus

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

Make rs63751653(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37011862

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751653
dbSNP (classic)	rs63751653
ClinGen	rs63751653
ebi	rs63751653
HLI	rs63751653
Exac	rs63751653
Gnomad	rs63751653
Varsome	rs63751653
LitVar	rs63751653
Map	rs63751653
PheGenI	rs63751653
Biobank	rs63751653
1000 genomes	rs63751653
hgdp	rs63751653
ensembl	rs63751653
geneview	rs63751653
scholar	rs63751653
google	rs63751653
pharmgkb	rs63751653
gwascentral	rs63751653
openSNP	rs63751653
23andMe	rs63751653
SNPshot	rs63751653
SNPdbe	rs63751653
MSV3d	rs63751653
GWAS Ctlg	rs63751653

Max Magnitude

6

ClinVar
Risk	rs63751653(-;-)
Alt	rs63751653(-;-)
Reference	Rs63751653(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37053353delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075776.2,