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rs547662164

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs547662164(C;T)
Make rs547662164(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome5
is asnp
is mentioned by
dbSNPrs547662164
ebirs547662164
HLIrs547662164
Exacrs547662164
Varsomers547662164
Maprs547662164
PheGenIrs547662164
hapmaprs547662164
1000 genomesrs547662164
hgdprs547662164
ensemblrs547662164
gopubmedrs547662164
geneviewrs547662164
scholarrs547662164
googlers547662164
pharmgkbrs547662164
gwascentralrs547662164
openSNPrs547662164
23andMers547662164
23andMe allrs547662164
SNP Nexus

SNPshotrs547662164
SNPdbers547662164
MSV3drs547662164
GWAS Ctlgrs547662164
Max Magnitude0
ClinVar
Risk rs547662164(T;T)
Alt rs547662164(T;T)
Reference rs547662164(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MCCC2
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.70900248C>T
CLNSRC
CLNACC RCV000186000.1,