rs63751266

Orientation

plus

Stabilized

plus

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

Make rs63751266(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36996663

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751266
dbSNP (classic)	rs63751266
ClinGen	rs63751266
ebi	rs63751266
HLI	rs63751266
Exac	rs63751266
Gnomad	rs63751266
Varsome	rs63751266
LitVar	rs63751266
Map	rs63751266
PheGenI	rs63751266
Biobank	rs63751266
1000 genomes	rs63751266
hgdp	rs63751266
ensembl	rs63751266
geneview	rs63751266
scholar	rs63751266
google	rs63751266
pharmgkb	rs63751266
gwascentral	rs63751266
openSNP	rs63751266
23andMe	rs63751266
SNPshot	rs63751266
SNPdbe	rs63751266
MSV3d	rs63751266
GWAS Ctlg	rs63751266

Max Magnitude

6

ClinVar
Risk	rs63751266(-;-)
Alt	rs63751266(-;-)
Reference	Rs63751266(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37038154delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075280.2,