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rs387906910

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs387906910(C;G)
Make rs387906910(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position219210036
GeneABCB6, ZFAND2B
is asnp
is mentioned by
dbSNPrs387906910
ebirs387906910
HLIrs387906910
Exacrs387906910
Varsomers387906910
Maprs387906910
PheGenIrs387906910
hapmaprs387906910
1000 genomesrs387906910
hgdprs387906910
ensemblrs387906910
gopubmedrs387906910
geneviewrs387906910
scholarrs387906910
googlers387906910
pharmgkbrs387906910
gwascentralrs387906910
openSNPrs387906910
23andMers387906910
23andMe allrs387906910
SNP Nexus

SNPshotrs387906910
SNPdbers387906910
MSV3drs387906910
GWAS Ctlgrs387906910
Max Magnitude0
ClinVar
Risk rs387906910(G;G)
Alt rs387906910(G;G)
Reference rs387906910(C;C)
Significance Pathogenic
Disease Microphthalmia
Variation info
Gene ZFAND2B ABCB6
CLNDBN Microphthalmia, isolated, with coloboma 7
Reversed 1
HGVS NC_000002.11:g.220074758G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000023439.2,