rs63749795

Orientation

plus

Stabilized

plus

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

Make rs63749795(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37028833

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749795
dbSNP (classic)	rs63749795
ClinGen	rs63749795
ebi	rs63749795
HLI	rs63749795
Exac	rs63749795
Gnomad	rs63749795
Varsome	rs63749795
LitVar	rs63749795
Map	rs63749795
PheGenI	rs63749795
Biobank	rs63749795
1000 genomes	rs63749795
hgdp	rs63749795
ensembl	rs63749795
geneview	rs63749795
scholar	rs63749795
google	rs63749795
pharmgkb	rs63749795
gwascentral	rs63749795
openSNP	rs63749795
23andMe	rs63749795
SNPshot	rs63749795
SNPdbe	rs63749795
MSV3d	rs63749795
GWAS Ctlg	rs63749795

Max Magnitude

6

ClinVar
Risk	rs63749795(T;T)
Alt	rs63749795(T;T)
Reference	Rs63749795(C;C)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37070324C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075218.3, RCV000128870.3, RCV000255034.2,