rs63751608

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;T)	6	Lynch syndrome, pathogenic mutation
(T;T)	0	common in clinvar

Make rs63751608(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37042321

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751608
dbSNP (classic)	rs63751608
ClinGen	rs63751608
ebi	rs63751608
HLI	rs63751608
Exac	rs63751608
Gnomad	rs63751608
Varsome	rs63751608
LitVar	rs63751608
Map	rs63751608
PheGenI	rs63751608
Biobank	rs63751608
1000 genomes	rs63751608
hgdp	rs63751608
ensembl	rs63751608
geneview	rs63751608
scholar	rs63751608
google	rs63751608
pharmgkb	rs63751608
gwascentral	rs63751608
openSNP	rs63751608
23andMe	rs63751608
SNPshot	rs63751608
SNPdbe	rs63751608
MSV3d	rs63751608
GWAS Ctlg	rs63751608

Max Magnitude

6

ClinVar
Risk	rs63751608(C;C)
Alt	rs63751608(C;C)
Reference	Rs63751608(T;T)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37083812T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075320.2,