rs63751200

Orientation

plus

Stabilized

plus

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

Make rs63751200(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37048596

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751200
dbSNP (classic)	rs63751200
ClinGen	rs63751200
ebi	rs63751200
HLI	rs63751200
Exac	rs63751200
Gnomad	rs63751200
Varsome	rs63751200
LitVar	rs63751200
Map	rs63751200
PheGenI	rs63751200
Biobank	rs63751200
1000 genomes	rs63751200
hgdp	rs63751200
ensembl	rs63751200
geneview	rs63751200
scholar	rs63751200
google	rs63751200
pharmgkb	rs63751200
gwascentral	rs63751200
openSNP	rs63751200
23andMe	rs63751200
SNPshot	rs63751200
SNPdbe	rs63751200
MSV3d	rs63751200
GWAS Ctlg	rs63751200

Max Magnitude

6

ClinVar
Risk	rs63751200(-;-)
Alt	rs63751200(-;-)
Reference	Rs63751200(GA;GA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37090087_37090088delGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075449.2,