rs63750020

Orientation

plus

Stabilized

plus

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

Make rs63750020(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025975

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750020
dbSNP (classic)	rs63750020
ClinGen	rs63750020
ebi	rs63750020
HLI	rs63750020
Exac	rs63750020
Gnomad	rs63750020
Varsome	rs63750020
LitVar	rs63750020
Map	rs63750020
PheGenI	rs63750020
Biobank	rs63750020
1000 genomes	rs63750020
hgdp	rs63750020
ensembl	rs63750020
geneview	rs63750020
scholar	rs63750020
google	rs63750020
pharmgkb	rs63750020
gwascentral	rs63750020
openSNP	rs63750020
23andMe	rs63750020
SNPshot	rs63750020
SNPdbe	rs63750020
MSV3d	rs63750020
GWAS Ctlg	rs63750020

Max Magnitude

6

ClinVar
Risk	rs63750020(A;A)
Alt	rs63750020(A;A)
Reference	Rs63750020(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067466dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075183.2,