rs63750658

Orientation

plus

Stabilized

plus

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

Make rs63750658(AA;AA)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37004449

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750658
dbSNP (classic)	rs63750658
ClinGen	rs63750658
ebi	rs63750658
HLI	rs63750658
Exac	rs63750658
Gnomad	rs63750658
Varsome	rs63750658
LitVar	rs63750658
Map	rs63750658
PheGenI	rs63750658
Biobank	rs63750658
1000 genomes	rs63750658
hgdp	rs63750658
ensembl	rs63750658
geneview	rs63750658
scholar	rs63750658
google	rs63750658
pharmgkb	rs63750658
gwascentral	rs63750658
openSNP	rs63750658
23andMe	rs63750658
SNPshot	rs63750658
SNPdbe	rs63750658
MSV3d	rs63750658
GWAS Ctlg	rs63750658

Max Magnitude

6

ClinVar
Risk	rs63750658(AA;AA)
Alt	rs63750658(AA;AA)
Reference	Rs63750658(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37045939_37045940dupAA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075667.2,