Have questions? Visit https://www.reddit.com/r/SNPedia

rs367548363

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs367548363(G;T)
Make rs367548363(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position123256826
GeneC12orf65, LOC105370040
is asnp
is mentioned by
dbSNPrs367548363
ebirs367548363
HLIrs367548363
Exacrs367548363
Varsomers367548363
Maprs367548363
PheGenIrs367548363
hapmaprs367548363
1000 genomesrs367548363
hgdprs367548363
ensemblrs367548363
gopubmedrs367548363
geneviewrs367548363
scholarrs367548363
googlers367548363
pharmgkbrs367548363
gwascentralrs367548363
openSNPrs367548363
23andMers367548363
23andMe allrs367548363
SNP Nexus

SNPshotrs367548363
SNPdbers367548363
MSV3drs367548363
GWAS Ctlgrs367548363
Max Magnitude0
ClinVar
Risk rs367548363(A,T;A,T)
Alt rs367548363(A,T;A,T)
Reference rs367548363(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene C12orf65
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.123741373G>T
CLNSRC
CLNACC RCV000198302.1,