rs63750726

Orientation

plus

Stabilized

plus

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

Make rs63750726(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048581

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750726
dbSNP (classic)	rs63750726
ClinGen	rs63750726
ebi	rs63750726
HLI	rs63750726
Exac	rs63750726
Gnomad	rs63750726
Varsome	rs63750726
LitVar	rs63750726
Map	rs63750726
PheGenI	rs63750726
Biobank	rs63750726
1000 genomes	rs63750726
hgdp	rs63750726
ensembl	rs63750726
geneview	rs63750726
scholar	rs63750726
google	rs63750726
pharmgkb	rs63750726
gwascentral	rs63750726
openSNP	rs63750726
23andMe	rs63750726
SNPshot	rs63750726
SNPdbe	rs63750726
MSV3d	rs63750726
GWAS Ctlg	rs63750726

Max Magnitude

6

ClinVar
Risk	rs63750726(T;T)
Alt	rs63750726(T;T)
Reference	Rs63750726(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000003.11:g.37090072C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075439.2, RCV000215855.1,