rs63750386

Orientation

plus

Stabilized

plus

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

Make rs63750386(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047597

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750386
dbSNP (classic)	rs63750386
ClinGen	rs63750386
ebi	rs63750386
HLI	rs63750386
Exac	rs63750386
Gnomad	rs63750386
Varsome	rs63750386
LitVar	rs63750386
Map	rs63750386
PheGenI	rs63750386
Biobank	rs63750386
1000 genomes	rs63750386
hgdp	rs63750386
ensembl	rs63750386
geneview	rs63750386
scholar	rs63750386
google	rs63750386
pharmgkb	rs63750386
gwascentral	rs63750386
openSNP	rs63750386
23andMe	rs63750386
SNPshot	rs63750386
SNPdbe	rs63750386
MSV3d	rs63750386
GWAS Ctlg	rs63750386

Max Magnitude

6

ClinVar
Risk	rs63750386(T;T)
Alt	rs63750386(T;T)
Reference	Rs63750386(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089088A>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075370.2,