rs63750889

Orientation

plus

Stabilized

plus

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

Make rs63750889(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37017566

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750889
dbSNP (classic)	rs63750889
ClinGen	rs63750889
ebi	rs63750889
HLI	rs63750889
Exac	rs63750889
Gnomad	rs63750889
Varsome	rs63750889
LitVar	rs63750889
Map	rs63750889
PheGenI	rs63750889
Biobank	rs63750889
1000 genomes	rs63750889
hgdp	rs63750889
ensembl	rs63750889
geneview	rs63750889
scholar	rs63750889
google	rs63750889
pharmgkb	rs63750889
gwascentral	rs63750889
openSNP	rs63750889
23andMe	rs63750889
SNPshot	rs63750889
SNPdbe	rs63750889
MSV3d	rs63750889
GWAS Ctlg	rs63750889

Max Magnitude

6

ClinVar
Risk	rs63750889(A;A)
Alt	rs63750889(A;A)
Reference	Rs63750889(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37059057T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075886.2,