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rs369698072

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369698072(A;A)
Make rs369698072(A;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position15238670
GeneNBAS
is asnp
is mentioned by
dbSNPrs369698072
ebirs369698072
HLIrs369698072
Exacrs369698072
Varsomers369698072
Maprs369698072
PheGenIrs369698072
hapmaprs369698072
1000 genomesrs369698072
hgdprs369698072
ensemblrs369698072
gopubmedrs369698072
geneviewrs369698072
scholarrs369698072
googlers369698072
pharmgkbrs369698072
gwascentralrs369698072
openSNPrs369698072
23andMers369698072
23andMe allrs369698072
SNP Nexus

SNPshotrs369698072
SNPdbers369698072
MSV3drs369698072
GWAS Ctlgrs369698072
Max Magnitude0
ClinVar
Risk rs369698072(A,T;A,T)
Alt rs369698072(A,T;A,T)
Reference rs369698072(C;C)
Significance Pathogenic
Disease Short stature
Variation info
Gene NBAS
CLNDBN Short stature, optic nerve atrophy, and pelger-huet anomaly
Reversed 0
HGVS NC_000002.11:g.15378794C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030702.2,