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rs397514584

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397514584(A;G)
Make rs397514584(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position77902641
GeneCOX7B
is asnp
is mentioned by
dbSNPrs397514584
ebirs397514584
HLIrs397514584
Exacrs397514584
Varsomers397514584
Maprs397514584
PheGenIrs397514584
hapmaprs397514584
1000 genomesrs397514584
hgdprs397514584
ensemblrs397514584
gopubmedrs397514584
geneviewrs397514584
scholarrs397514584
googlers397514584
pharmgkbrs397514584
gwascentralrs397514584
openSNPrs397514584
23andMers397514584
23andMe allrs397514584
SNP Nexus

SNPshotrs397514584
SNPdbers397514584
MSV3drs397514584
GWAS Ctlgrs397514584
Max Magnitude0
ClinVar
Risk rs397514584(G;G)
Alt rs397514584(G;G)
Reference rs397514584(A;A)
Significance Pathogenic
Disease Linear skin defects with multiple congenital anomalies 2
Variation info
Gene COX7B
CLNDBN Linear skin defects with multiple congenital anomalies 2
Reversed 0
HGVS NC_000023.10:g.77158138A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000032987.7,