rs63750484

Orientation

plus

Stabilized

plus

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

Make rs63750484(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37050545

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750484
dbSNP (classic)	rs63750484
ClinGen	rs63750484
ebi	rs63750484
HLI	rs63750484
Exac	rs63750484
Gnomad	rs63750484
Varsome	rs63750484
LitVar	rs63750484
Map	rs63750484
PheGenI	rs63750484
Biobank	rs63750484
1000 genomes	rs63750484
hgdp	rs63750484
ensembl	rs63750484
geneview	rs63750484
scholar	rs63750484
google	rs63750484
pharmgkb	rs63750484
gwascentral	rs63750484
openSNP	rs63750484
23andMe	rs63750484
SNPshot	rs63750484
SNPdbe	rs63750484
MSV3d	rs63750484
GWAS Ctlg	rs63750484

Max Magnitude

6

ClinVar
Risk	rs63750484(A;A)
Alt	rs63750484(A;A)
Reference	Rs63750484(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37092036T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075565.2,