rs63750903

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(AT;GG)	6	Lynch syndrome, pathogenic mutation
(CT;GG)	6	Lynch syndrome, pathogenic mutation
(GG;GG)	0	common in clinvar
(TGG;TGG)	0	common in clinvar

Make rs63750903(CT;CT)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37008891

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750903
dbSNP (classic)	rs63750903
ClinGen	rs63750903
ebi	rs63750903
HLI	rs63750903
Exac	rs63750903
Gnomad	rs63750903
Varsome	rs63750903
LitVar	rs63750903
Map	rs63750903
PheGenI	rs63750903
Biobank	rs63750903
1000 genomes	rs63750903
hgdp	rs63750903
ensembl	rs63750903
geneview	rs63750903
scholar	rs63750903
google	rs63750903
pharmgkb	rs63750903
gwascentral	rs63750903
openSNP	rs63750903
23andMe	rs63750903
SNPshot	rs63750903
SNPdbe	rs63750903
MSV3d	rs63750903
GWAS Ctlg	rs63750903

Max Magnitude

6

ClinVar
Risk	rs63750903(AT;AT) rs63750903(CT;CT)
Alt	rs63750903(AT;AT) rs63750903(CT;CT)
Reference	Rs63750903(GG;GG)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37050382_37050383delGGinsAT; NC_000003.11:g.37050382_37050383delGGinsCT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075744.2, RCV000482203.1, RCV000075745.2,