rs63749906

Orientation

plus

Stabilized

plus

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

Make rs63749906(G;G)

Reference

GRCh38 38.1/141

Chromosome

3

Position

36993651

Gene	EPM2AIP1, MLH1

is a	snp
is	mentioned by
dbSNP	rs63749906
dbSNP (classic)	rs63749906
ClinGen	rs63749906
ebi	rs63749906
HLI	rs63749906
Exac	rs63749906
Gnomad	rs63749906
Varsome	rs63749906
LitVar	rs63749906
Map	rs63749906
PheGenI	rs63749906
Biobank	rs63749906
1000 genomes	rs63749906
hgdp	rs63749906
ensembl	rs63749906
geneview	rs63749906
scholar	rs63749906
google	rs63749906
pharmgkb	rs63749906
gwascentral	rs63749906
openSNP	rs63749906
23andMe	rs63749906
SNPshot	rs63749906
SNPdbe	rs63749906
MSV3d	rs63749906
GWAS Ctlg	rs63749906

Max Magnitude

6

ClinVar
Risk	rs63749906(G;G)
Alt	rs63749906(G;G)
Reference	Rs63749906(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	EPM2AIP1 MLH1
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000003.11:g.37035142T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000075100.2,