rs63749990

Orientation

plus

Stabilized

plus

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

Make rs63749990(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

37000985

Gene

MLH1

is a	snp
is	mentioned by
dbSNP	rs63749990
dbSNP (classic)	rs63749990
ClinGen	rs63749990
ebi	rs63749990
HLI	rs63749990
Exac	rs63749990
Gnomad	rs63749990
Varsome	rs63749990
LitVar	rs63749990
Map	rs63749990
PheGenI	rs63749990
Biobank	rs63749990
1000 genomes	rs63749990
hgdp	rs63749990
ensembl	rs63749990
geneview	rs63749990
scholar	rs63749990
google	rs63749990
pharmgkb	rs63749990
gwascentral	rs63749990
openSNP	rs63749990
23andMe	rs63749990
SNPshot	rs63749990
SNPdbe	rs63749990
MSV3d	rs63749990
GWAS Ctlg	rs63749990

Max Magnitude

6

ClinVar
Risk	rs63749990(G;G)
Alt	rs63749990(G;G)
Reference	Rs63749990(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37042476T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075601.2,