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rs1064796339

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome20
Position50893869
GeneADNP
is asnp
is mentioned by
dbSNPrs1064796339
dbSNP (old)rs1064796339
ClinGenrs1064796339
ebirs1064796339
HLIrs1064796339
Exacrs1064796339
Gnomadrs1064796339
Varsomers1064796339
Maprs1064796339
PheGenIrs1064796339
Biobankrs1064796339
1000 genomesrs1064796339
hgdprs1064796339
ensemblrs1064796339
gopubmedrs1064796339
geneviewrs1064796339
scholarrs1064796339
googlers1064796339
pharmgkbrs1064796339
gwascentralrs1064796339
openSNPrs1064796339
23andMers1064796339
23andMe allrs1064796339
SNPshotrs1064796339
SNPdbers1064796339
MSV3drs1064796339
GWAS Ctlgrs1064796339
Max Magnitude0
ClinVar
Risk rs1064796339(-;-)
Alt rs1064796339(-;-)
Reference Rs1064796339(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene ADNP
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.49510406delC
CLNSRC
CLNACC RCV000484504.1,