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rs16892095

From SNPedia

Orientationplus
Make rs16892095(A;A)
Make rs16892095(A;C)
Make rs16892095(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position15516734
GeneCC2D2A
is asnp
is mentioned by
dbSNPrs16892095
ebirs16892095
HLIrs16892095
Exacrs16892095
Varsomers16892095
Maprs16892095
PheGenIrs16892095
hapmaprs16892095
1000 genomesrs16892095
hgdprs16892095
ensemblrs16892095
gopubmedrs16892095
geneviewrs16892095
scholarrs16892095
googlers16892095
pharmgkbrs16892095
gwascentralrs16892095
openSNPrs16892095
23andMers16892095
23andMe allrs16892095
SNP Nexus

SNPshotrs16892095
SNPdbers16892095
MSV3drs16892095
GWAS Ctlgrs16892095
Max Magnitude
? (A;A) (A;C) (C;C) 28
ClinVar
Risk rs16892095(C;C)
Alt rs16892095(C;C)
Reference rs16892095(A;A)
Significance Other
Disease not specified
Variation info
Gene CC2D2A
CLNDBN not specified
Reversed 0
HGVS NC_000004.11:g.15518357A>C
CLNSRC
CLNACC RCV000114163.3,