rs63750115

Orientation

plus

Stabilized

plus

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

Make rs63750115(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048591

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750115
dbSNP (classic)	rs63750115
ClinGen	rs63750115
ebi	rs63750115
HLI	rs63750115
Exac	rs63750115
Gnomad	rs63750115
Varsome	rs63750115
LitVar	rs63750115
Map	rs63750115
PheGenI	rs63750115
Biobank	rs63750115
1000 genomes	rs63750115
hgdp	rs63750115
ensembl	rs63750115
geneview	rs63750115
scholar	rs63750115
google	rs63750115
pharmgkb	rs63750115
gwascentral	rs63750115
openSNP	rs63750115
23andMe	rs63750115
SNPshot	rs63750115
SNPdbe	rs63750115
MSV3d	rs63750115
GWAS Ctlg	rs63750115

Max Magnitude

6

ClinVar
Risk	rs63750115(-;-)
Alt	rs63750115(-;-)
Reference	Rs63750115(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090082delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075443.2,