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rs17472401

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs17472401(A;A)
Make rs17472401(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position5880183
GeneNPHP4
is asnp
is mentioned by
dbSNPrs17472401
dbSNP (classic)rs17472401
ClinGenrs17472401
ebirs17472401
HLIrs17472401
Exacrs17472401
Gnomadrs17472401
Varsomers17472401
LitVarrs17472401
Maprs17472401
PheGenIrs17472401
Biobankrs17472401
1000 genomesrs17472401
hgdprs17472401
ensemblrs17472401
geneviewrs17472401
scholarrs17472401
googlers17472401
pharmgkbrs17472401
gwascentralrs17472401
openSNPrs17472401
23andMers17472401
SNPshotrs17472401
SNPdbers17472401
MSV3drs17472401
GWAS Ctlgrs17472401
GMAF0.01194
Max Magnitude0
? (A;A) (A;G) (G;G) 28



ClinVar
Risk rs17472401(A;A)
Alt rs17472401(A;A)
Reference Rs17472401(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene NPHP4
CLNDBN not specified
Reversed 0
HGVS NC_000001.10:g.5940243G>A
CLNSRC HGMD UniProtKB (protein)
CLNACC RCV000081708.4,