rs63750483

Orientation

plus

Stabilized

plus

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

Make rs63750483(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025790

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750483
dbSNP (classic)	rs63750483
ClinGen	rs63750483
ebi	rs63750483
HLI	rs63750483
Exac	rs63750483
Gnomad	rs63750483
Varsome	rs63750483
LitVar	rs63750483
Map	rs63750483
PheGenI	rs63750483
Biobank	rs63750483
1000 genomes	rs63750483
hgdp	rs63750483
ensembl	rs63750483
geneview	rs63750483
scholar	rs63750483
google	rs63750483
pharmgkb	rs63750483
gwascentral	rs63750483
openSNP	rs63750483
23andMe	rs63750483
SNPshot	rs63750483
SNPdbe	rs63750483
MSV3d	rs63750483
GWAS Ctlg	rs63750483

Max Magnitude

6

ClinVar
Risk	rs63750483(G;G) rs63750483(T;T)
Alt	rs63750483(G;G) rs63750483(T;T)
Reference	Rs63750483(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067281C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075146.2,