rs63749965

Orientation

plus

Stabilized

plus

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

Make rs63749965(-;-)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37025748

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749965
dbSNP (classic)	rs63749965
ClinGen	rs63749965
ebi	rs63749965
HLI	rs63749965
Exac	rs63749965
Gnomad	rs63749965
Varsome	rs63749965
LitVar	rs63749965
Map	rs63749965
PheGenI	rs63749965
Biobank	rs63749965
1000 genomes	rs63749965
hgdp	rs63749965
ensembl	rs63749965
geneview	rs63749965
scholar	rs63749965
google	rs63749965
pharmgkb	rs63749965
gwascentral	rs63749965
openSNP	rs63749965
23andMe	rs63749965
SNPshot	rs63749965
SNPdbe	rs63749965
MSV3d	rs63749965
GWAS Ctlg	rs63749965

Max Magnitude

6

ClinVar
Risk	rs63749965(-;-)
Alt	rs63749965(-;-)
Reference	Rs63749965(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37067239delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075122.2,