rs63750819

Orientation

plus

Stabilized

plus

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

Make rs63750819(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37014499

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750819
dbSNP (classic)	rs63750819
ClinGen	rs63750819
ebi	rs63750819
HLI	rs63750819
Exac	rs63750819
Gnomad	rs63750819
Varsome	rs63750819
LitVar	rs63750819
Map	rs63750819
PheGenI	rs63750819
Biobank	rs63750819
1000 genomes	rs63750819
hgdp	rs63750819
ensembl	rs63750819
geneview	rs63750819
scholar	rs63750819
google	rs63750819
pharmgkb	rs63750819
gwascentral	rs63750819
openSNP	rs63750819
23andMe	rs63750819
SNPshot	rs63750819
SNPdbe	rs63750819
MSV3d	rs63750819
GWAS Ctlg	rs63750819

Max Magnitude

6

ClinVar
Risk	rs63750819(G;G)
Alt	rs63750819(G;G)
Reference	Rs63750819(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37055990dupG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075836.2,