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rs10262966

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs10262966(A;G)
Make rs10262966(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position75954007
GenePOR
is asnp
is mentioned by
dbSNPrs10262966
ebirs10262966
HLIrs10262966
Exacrs10262966
Varsomers10262966
Maprs10262966
PheGenIrs10262966
hapmaprs10262966
1000 genomesrs10262966
hgdprs10262966
ensemblrs10262966
gopubmedrs10262966
geneviewrs10262966
scholarrs10262966
googlers10262966
pharmgkbrs10262966
gwascentralrs10262966
openSNPrs10262966
23andMers10262966
23andMe allrs10262966
SNP Nexus

SNPshotrs10262966
SNPdbers10262966
MSV3drs10262966
GWAS Ctlgrs10262966
Max Magnitude0
ClinVar
Risk rs10262966(G;G)
Alt rs10262966(G;G)
Reference rs10262966(A;A)
Significance Pathogenic
Disease Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
Variation info
Gene POR
CLNDBN Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis
Reversed 0
HGVS NC_000007.13:g.75583325A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000018413.28,