Have questions? Visit https://www.reddit.com/r/SNPedia

rs672601304

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs672601304(A;G)
Make rs672601304(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position109483552
GeneUBE3B
is asnp
is mentioned by
dbSNPrs672601304
ebirs672601304
HLIrs672601304
Exacrs672601304
Varsomers672601304
Maprs672601304
PheGenIrs672601304
hapmaprs672601304
1000 genomesrs672601304
hgdprs672601304
ensemblrs672601304
gopubmedrs672601304
geneviewrs672601304
scholarrs672601304
googlers672601304
pharmgkbrs672601304
gwascentralrs672601304
openSNPrs672601304
23andMers672601304
23andMe allrs672601304
SNP Nexus

SNPshotrs672601304
SNPdbers672601304
MSV3drs672601304
GWAS Ctlgrs672601304
Max Magnitude0
ClinVar
Risk rs672601304(G;G)
Alt rs672601304(G;G)
Reference rs672601304(A;A)
Significance Pathogenic
Disease Kaufman oculocerebrofacial syndrome
Variation info
Gene UBE3B
CLNDBN Kaufman oculocerebrofacial syndrome
Reversed 0
HGVS NC_000012.11:g.109921357A>G
CLNSRC VariO
CLNACC RCV000149398.1,