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rs374805348

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374805348(A;A)
Make rs374805348(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position93625654
GenePDE6C
is asnp
is mentioned by
dbSNPrs374805348
ebirs374805348
HLIrs374805348
Exacrs374805348
Varsomers374805348
Maprs374805348
PheGenIrs374805348
hapmaprs374805348
1000 genomesrs374805348
hgdprs374805348
ensemblrs374805348
gopubmedrs374805348
geneviewrs374805348
scholarrs374805348
googlers374805348
pharmgkbrs374805348
gwascentralrs374805348
openSNPrs374805348
23andMers374805348
23andMe allrs374805348
SNP Nexus

SNPshotrs374805348
SNPdbers374805348
MSV3drs374805348
GWAS Ctlgrs374805348
Max Magnitude0
ClinVar
Risk rs374805348(A;A)
Alt rs374805348(A;A)
Reference rs374805348(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PDE6C
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.95385411G>A
CLNSRC
CLNACC RCV000171185.1,