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

rs199517715

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199517715(C;T)
Make rs199517715(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position183092545
GeneMCCC1
is asnp
is mentioned by
dbSNPrs199517715
ebirs199517715
HLIrs199517715
Exacrs199517715
Varsomers199517715
Maprs199517715
PheGenIrs199517715
hapmaprs199517715
1000 genomesrs199517715
hgdprs199517715
ensemblrs199517715
gopubmedrs199517715
geneviewrs199517715
scholarrs199517715
googlers199517715
pharmgkbrs199517715
gwascentralrs199517715
openSNPrs199517715
23andMers199517715
23andMe allrs199517715
SNP Nexus

SNPshotrs199517715
SNPdbers199517715
MSV3drs199517715
GWAS Ctlgrs199517715
Max Magnitude0
ClinVar
Risk rs199517715(T;T)
Alt rs199517715(T;T)
Reference rs199517715(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC1
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.182810333C>T
CLNSRC
CLNACC RCV000185992.1,