rs63750293

Orientation

plus

Stabilized

plus

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

Make rs63750293(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025859

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750293
dbSNP (classic)	rs63750293
ClinGen	rs63750293
ebi	rs63750293
HLI	rs63750293
Exac	rs63750293
Gnomad	rs63750293
Varsome	rs63750293
LitVar	rs63750293
Map	rs63750293
PheGenI	rs63750293
Biobank	rs63750293
1000 genomes	rs63750293
hgdp	rs63750293
ensembl	rs63750293
geneview	rs63750293
scholar	rs63750293
google	rs63750293
pharmgkb	rs63750293
gwascentral	rs63750293
openSNP	rs63750293
23andMe	rs63750293
SNPshot	rs63750293
SNPdbe	rs63750293
MSV3d	rs63750293
GWAS Ctlg	rs63750293

Max Magnitude

6

ClinVar
Risk	rs63750293(-;-)
Alt	rs63750293(-;-)
Reference	Rs63750293(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067350delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075162.2,