rs63750865

Orientation

plus

Stabilized

plus

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

Make rs63750865(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37006992

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63750865
dbSNP (classic)	rs63750865
ClinGen	rs63750865
ebi	rs63750865
HLI	rs63750865
Exac	rs63750865
Gnomad	rs63750865
Varsome	rs63750865
LitVar	rs63750865
Map	rs63750865
PheGenI	rs63750865
Biobank	rs63750865
1000 genomes	rs63750865
hgdp	rs63750865
ensembl	rs63750865
geneview	rs63750865
scholar	rs63750865
google	rs63750865
pharmgkb	rs63750865
gwascentral	rs63750865
openSNP	rs63750865
23andMe	rs63750865
SNPshot	rs63750865
SNPdbe	rs63750865
MSV3d	rs63750865
GWAS Ctlg	rs63750865

Max Magnitude

6

ClinVar
Risk	rs63750865(-;-)
Alt	rs63750865(-;-)
Reference	Rs63750865(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37048483delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075689.2,