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rs552219028

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs552219028(A;C)
Make rs552219028(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome4
Position122923143
GeneNUDT6, SPATA5
is asnp
is mentioned by
dbSNPrs552219028
ebirs552219028
HLIrs552219028
Exacrs552219028
Varsomers552219028
Maprs552219028
PheGenIrs552219028
hapmaprs552219028
1000 genomesrs552219028
hgdprs552219028
ensemblrs552219028
gopubmedrs552219028
geneviewrs552219028
scholarrs552219028
googlers552219028
pharmgkbrs552219028
gwascentralrs552219028
openSNPrs552219028
23andMers552219028
23andMe allrs552219028
SNP Nexus

SNPshotrs552219028
SNPdbers552219028
MSV3drs552219028
GWAS Ctlgrs552219028
Max Magnitude0
ClinVar
Risk rs552219028(C,G,T;C,G,T)
Alt rs552219028(C,G,T;C,G,T)
Reference rs552219028(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene NUDT6 SPATA5
CLNDBN not provided
Reversed 0
HGVS NC_000004.11:g.123844298A>C
CLNSRC
CLNACC RCV000185657.1,