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rs121908164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121908164(A;A)
Make rs121908164(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position10365476
GeneKIF1B, LOC105376725
is asnp
is mentioned by
dbSNPrs121908164
dbSNP (classic)rs121908164
ClinGenrs121908164
ebirs121908164
HLIrs121908164
Exacrs121908164
Gnomadrs121908164
Varsomers121908164
LitVarrs121908164
Maprs121908164
PheGenIrs121908164
Biobankrs121908164
1000 genomesrs121908164
hgdprs121908164
ensemblrs121908164
geneviewrs121908164
scholarrs121908164
googlers121908164
pharmgkbrs121908164
gwascentralrs121908164
openSNPrs121908164
23andMers121908164
SNPshotrs121908164
SNPdbers121908164
MSV3drs121908164
GWAS Ctlgrs121908164
Max Magnitude0
OMIM605995
Desc
Variant0005
Relatedalso
ClinVar
Risk rs121908164(A;A)
Alt rs121908164(A;A)
Reference Rs121908164(G;G)
Significance Other
Disease Pheochromocytoma Neuroblastoma 1
Variation info
Gene KIF1B
CLNDBN Pheochromocytoma Neuroblastoma 1
Reversed 0
HGVS NC_000001.10:g.10425534G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000004925.2, RCV000004926.2,