rs63750028

Orientation

plus

Stabilized

plus

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

Make rs63750028(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996658

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750028
dbSNP (classic)	rs63750028
ClinGen	rs63750028
ebi	rs63750028
HLI	rs63750028
Exac	rs63750028
Gnomad	rs63750028
Varsome	rs63750028
LitVar	rs63750028
Map	rs63750028
PheGenI	rs63750028
Biobank	rs63750028
1000 genomes	rs63750028
hgdp	rs63750028
ensembl	rs63750028
geneview	rs63750028
scholar	rs63750028
google	rs63750028
pharmgkb	rs63750028
gwascentral	rs63750028
openSNP	rs63750028
23andMe	rs63750028
SNPshot	rs63750028
SNPdbe	rs63750028
MSV3d	rs63750028
GWAS Ctlg	rs63750028

Max Magnitude

6

ClinVar
Risk	rs63750028(A;A)
Alt	rs63750028(A;A)
Reference	Rs63750028(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038149dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075268.2,