rs63750639

Orientation

plus

Stabilized

plus

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

Make rs63750639(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048912

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750639
dbSNP (classic)	rs63750639
ClinGen	rs63750639
ebi	rs63750639
HLI	rs63750639
Exac	rs63750639
Gnomad	rs63750639
Varsome	rs63750639
LitVar	rs63750639
Map	rs63750639
PheGenI	rs63750639
Biobank	rs63750639
1000 genomes	rs63750639
hgdp	rs63750639
ensembl	rs63750639
geneview	rs63750639
scholar	rs63750639
google	rs63750639
pharmgkb	rs63750639
gwascentral	rs63750639
openSNP	rs63750639
23andMe	rs63750639
SNPshot	rs63750639
SNPdbe	rs63750639
MSV3d	rs63750639
GWAS Ctlg	rs63750639

Max Magnitude

6

ClinVar
Risk	rs63750639(A;A)
Alt	rs63750639(A;A)
Reference	Rs63750639(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090403G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075473.2,