rs63751259

Orientation

plus

Stabilized

plus

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

Make rs63751259(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37020364

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751259
dbSNP (classic)	rs63751259
ClinGen	rs63751259
ebi	rs63751259
HLI	rs63751259
Exac	rs63751259
Gnomad	rs63751259
Varsome	rs63751259
LitVar	rs63751259
Map	rs63751259
PheGenI	rs63751259
Biobank	rs63751259
1000 genomes	rs63751259
hgdp	rs63751259
ensembl	rs63751259
geneview	rs63751259
scholar	rs63751259
google	rs63751259
pharmgkb	rs63751259
gwascentral	rs63751259
openSNP	rs63751259
23andMe	rs63751259
SNPshot	rs63751259
SNPdbe	rs63751259
MSV3d	rs63751259
GWAS Ctlg	rs63751259

Max Magnitude

6

ClinVar
Risk	rs63751259(A;A)
Alt	rs63751259(A;A)
Reference	Rs63751259(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37061855dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075942.2,