rs63750891

Orientation

plus

Stabilized

plus

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

Make rs63750891(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37008824

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750891
dbSNP (classic)	rs63750891
ClinGen	rs63750891
ebi	rs63750891
HLI	rs63750891
Exac	rs63750891
Gnomad	rs63750891
Varsome	rs63750891
LitVar	rs63750891
Map	rs63750891
PheGenI	rs63750891
Biobank	rs63750891
1000 genomes	rs63750891
hgdp	rs63750891
ensembl	rs63750891
geneview	rs63750891
scholar	rs63750891
google	rs63750891
pharmgkb	rs63750891
gwascentral	rs63750891
openSNP	rs63750891
23andMe	rs63750891
SNPshot	rs63750891
SNPdbe	rs63750891
MSV3d	rs63750891
GWAS Ctlg	rs63750891

Max Magnitude

6

ClinVar
Risk	rs63750891(G;G)
Alt	rs63750891(G;G)
Reference	Rs63750891(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37050315T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075730.2,