rs63750282

Orientation

plus

Stabilized

plus

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

Make rs63750282(A;A)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048914

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750282
dbSNP (classic)	rs63750282
ClinGen	rs63750282
ebi	rs63750282
HLI	rs63750282
Exac	rs63750282
Gnomad	rs63750282
Varsome	rs63750282
LitVar	rs63750282
Map	rs63750282
PheGenI	rs63750282
Biobank	rs63750282
1000 genomes	rs63750282
hgdp	rs63750282
ensembl	rs63750282
geneview	rs63750282
scholar	rs63750282
google	rs63750282
pharmgkb	rs63750282
gwascentral	rs63750282
openSNP	rs63750282
23andMe	rs63750282
SNPshot	rs63750282
SNPdbe	rs63750282
MSV3d	rs63750282
GWAS Ctlg	rs63750282

Max Magnitude

6

ClinVar
Risk	rs63750282(A;A)
Alt	rs63750282(A;A)
Reference	Rs63750282(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090405dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075478.2,