rs63751685

Orientation

plus

Stabilized

plus

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

Make rs63751685(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37042325

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63751685
dbSNP (classic)	rs63751685
ClinGen	rs63751685
ebi	rs63751685
HLI	rs63751685
Exac	rs63751685
Gnomad	rs63751685
Varsome	rs63751685
LitVar	rs63751685
Map	rs63751685
PheGenI	rs63751685
Biobank	rs63751685
1000 genomes	rs63751685
hgdp	rs63751685
ensembl	rs63751685
geneview	rs63751685
scholar	rs63751685
google	rs63751685
pharmgkb	rs63751685
gwascentral	rs63751685
openSNP	rs63751685
23andMe	rs63751685
SNPshot	rs63751685
SNPdbe	rs63751685
MSV3d	rs63751685
GWAS Ctlg	rs63751685

Max Magnitude

6

ClinVar
Risk	rs63751685(-;-)
Alt	rs63751685(-;-)
Reference	Rs63751685(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37083816delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075321.2,