rs63750071

Orientation

plus

Stabilized

plus

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

Make rs63750071(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025952

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750071
dbSNP (classic)	rs63750071
ClinGen	rs63750071
ebi	rs63750071
HLI	rs63750071
Exac	rs63750071
Gnomad	rs63750071
Varsome	rs63750071
LitVar	rs63750071
Map	rs63750071
PheGenI	rs63750071
Biobank	rs63750071
1000 genomes	rs63750071
hgdp	rs63750071
ensembl	rs63750071
geneview	rs63750071
scholar	rs63750071
google	rs63750071
pharmgkb	rs63750071
gwascentral	rs63750071
openSNP	rs63750071
23andMe	rs63750071
SNPshot	rs63750071
SNPdbe	rs63750071
MSV3d	rs63750071
GWAS Ctlg	rs63750071

Max Magnitude

6

ClinVar
Risk	rs63750071(-;-)
Alt	rs63750071(-;-)
Reference	Rs63750071(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067443delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075178.2,