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rs774425075

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs774425075(C;T)
Make rs774425075(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position55680855
GenePNPT1
is asnp
is mentioned by
dbSNPrs774425075
dbSNP (classic)rs774425075
ClinGenrs774425075
ebirs774425075
HLIrs774425075
Exacrs774425075
Gnomadrs774425075
Varsomers774425075
LitVarrs774425075
Maprs774425075
PheGenIrs774425075
Biobankrs774425075
1000 genomesrs774425075
hgdprs774425075
ensemblrs774425075
geneviewrs774425075
scholarrs774425075
googlers774425075
pharmgkbrs774425075
gwascentralrs774425075
openSNPrs774425075
23andMers774425075
23andMe allrs774425075
SNPshotrs774425075
SNPdbers774425075
MSV3drs774425075
GWAS Ctlgrs774425075
Max Magnitude0
ClinVar
Risk rs774425075(T;T)
Alt rs774425075(T;T)
Reference Rs774425075(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PNPT1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.55907990C>T
CLNSRC
CLNACC RCV000489241.1,