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rs1057518345

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TTAG;TTAG) 0 common in clinvar
Make rs1057518345(-;-)
Make rs1057518345(-;TTAG)
ReferenceGRCh38.p7 38.3/150
Chromosome20
Position50894172
GeneADNP
is asnp
is mentioned by
dbSNPrs1057518345
dbSNP (old)rs1057518345
ClinGenrs1057518345
ebirs1057518345
HLIrs1057518345
Exacrs1057518345
Gnomadrs1057518345
Varsomers1057518345
Maprs1057518345
PheGenIrs1057518345
Biobankrs1057518345
1000 genomesrs1057518345
hgdprs1057518345
ensemblrs1057518345
gopubmedrs1057518345
geneviewrs1057518345
scholarrs1057518345
googlers1057518345
pharmgkbrs1057518345
gwascentralrs1057518345
openSNPrs1057518345
23andMers1057518345
23andMe allrs1057518345
SNPshotrs1057518345
SNPdbers1057518345
MSV3drs1057518345
GWAS Ctlgrs1057518345
Max Magnitude0
ClinVar
Risk rs1057518345(-;-)
Alt rs1057518345(-;-)
Reference Rs1057518345(TTAG;TTAG)
Significance Pathogenic
Disease not provided
Variation info
Gene ADNP
CLNDBN not provided
Reversed 1
HGVS NC_000020.10:g.49510709_49510712delCTAA
CLNSRC
CLNACC RCV000413777.1,