rs63750603

Orientation

plus

Stabilized

plus

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

Make rs63750603(C;C)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37049017

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750603
dbSNP (classic)	rs63750603
ClinGen	rs63750603
ebi	rs63750603
HLI	rs63750603
Exac	rs63750603
Gnomad	rs63750603
Varsome	rs63750603
LitVar	rs63750603
Map	rs63750603
PheGenI	rs63750603
Biobank	rs63750603
1000 genomes	rs63750603
hgdp	rs63750603
ensembl	rs63750603
geneview	rs63750603
scholar	rs63750603
google	rs63750603
pharmgkb	rs63750603
gwascentral	rs63750603
openSNP	rs63750603
23andMe	rs63750603
SNPshot	rs63750603
SNPdbe	rs63750603
MSV3d	rs63750603
GWAS Ctlg	rs63750603

Max Magnitude

6

ClinVar
Risk	rs63750603(A;A) rs63750603(C;C)
Alt	rs63750603(A;A) rs63750603(C;C)
Reference	Rs63750603(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090508G>A; NC_000003.11:g.37090508G>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075533.2, RCV000075534.2,