rs63751606

Orientation

plus

Stabilized

plus

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

Make rs63751606(C;T)

Make rs63751606(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37004472

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751606
dbSNP (classic)	rs63751606
ClinGen	rs63751606
ebi	rs63751606
HLI	rs63751606
Exac	rs63751606
Gnomad	rs63751606
Varsome	rs63751606
LitVar	rs63751606
Map	rs63751606
PheGenI	rs63751606
Biobank	rs63751606
1000 genomes	rs63751606
hgdp	rs63751606
ensembl	rs63751606
geneview	rs63751606
scholar	rs63751606
google	rs63751606
pharmgkb	rs63751606
gwascentral	rs63751606
openSNP	rs63751606
23andMe	rs63751606
SNPshot	rs63751606
SNPdbe	rs63751606
MSV3d	rs63751606
GWAS Ctlg	rs63751606

Max Magnitude

6

ClinVar
Risk	rs63751606(G;G) rs63751606(T;T)
Alt	rs63751606(G;G) rs63751606(T;T)
Reference	Rs63751606(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37045963C>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075674.2,