rs63750152

Orientation

plus

Stabilized

plus

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

Make rs63750152(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047664

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750152
dbSNP (classic)	rs63750152
ClinGen	rs63750152
ebi	rs63750152
HLI	rs63750152
Exac	rs63750152
Gnomad	rs63750152
Varsome	rs63750152
LitVar	rs63750152
Map	rs63750152
PheGenI	rs63750152
Biobank	rs63750152
1000 genomes	rs63750152
hgdp	rs63750152
ensembl	rs63750152
geneview	rs63750152
scholar	rs63750152
google	rs63750152
pharmgkb	rs63750152
gwascentral	rs63750152
openSNP	rs63750152
23andMe	rs63750152
SNPshot	rs63750152
SNPdbe	rs63750152
MSV3d	rs63750152
GWAS Ctlg	rs63750152

Max Magnitude

6

ClinVar
Risk	rs63750152(-;-)
Alt	rs63750152(-;-)
Reference	Rs63750152(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089155delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075396.2,