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rs398122968

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398122968(A;A)
Make rs398122968(A;G)
ReferenceGRCh38 38.1/141
Chromosome16
Position2499425
GeneTBC1D24
is asnp
is mentioned by
dbSNPrs398122968
ebirs398122968
HLIrs398122968
Exacrs398122968
Varsomers398122968
Maprs398122968
PheGenIrs398122968
hapmaprs398122968
1000 genomesrs398122968
hgdprs398122968
ensemblrs398122968
gopubmedrs398122968
geneviewrs398122968
scholarrs398122968
googlers398122968
pharmgkbrs398122968
gwascentralrs398122968
openSNPrs398122968
23andMers398122968
23andMe allrs398122968
SNP Nexus

SNPshotrs398122968
SNPdbers398122968
MSV3drs398122968
GWAS Ctlgrs398122968
Max Magnitude0
ClinVar
Risk rs398122968(A;A)
Alt rs398122968(A;A)
Reference rs398122968(G;G)
Significance Pathogenic
Disease Digitorenocerebral syndrome
Variation info
Gene TBC1D24
CLNDBN Digitorenocerebral syndrome
Reversed 0
HGVS NC_000016.9:g.2549426G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000076917.6,