rs63750150

Orientation

plus

Stabilized

plus

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

Make rs63750150(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37047618

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750150
dbSNP (classic)	rs63750150
ClinGen	rs63750150
ebi	rs63750150
HLI	rs63750150
Exac	rs63750150
Gnomad	rs63750150
Varsome	rs63750150
LitVar	rs63750150
Map	rs63750150
PheGenI	rs63750150
Biobank	rs63750150
1000 genomes	rs63750150
hgdp	rs63750150
ensembl	rs63750150
geneview	rs63750150
scholar	rs63750150
google	rs63750150
pharmgkb	rs63750150
gwascentral	rs63750150
openSNP	rs63750150
23andMe	rs63750150
SNPshot	rs63750150
SNPdbe	rs63750150
MSV3d	rs63750150
GWAS Ctlg	rs63750150

Max Magnitude

6

ClinVar
Risk	rs63750150(-;-)
Alt	rs63750150(-;-)
Reference	Rs63750150(AT;AT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37089109_37089110delAT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075376.2,