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rs587784231

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587784231(-;-)
Make rs587784231(-;A)
ReferenceGRCh38.p2 38.2/144
ChromosomeX
Position13756688
GeneOFD1
is asnp
is mentioned by
dbSNPrs587784231
ebirs587784231
HLIrs587784231
Exacrs587784231
Varsomers587784231
Maprs587784231
PheGenIrs587784231
hapmaprs587784231
1000 genomesrs587784231
hgdprs587784231
ensemblrs587784231
gopubmedrs587784231
geneviewrs587784231
scholarrs587784231
googlers587784231
pharmgkbrs587784231
gwascentralrs587784231
openSNPrs587784231
23andMers587784231
23andMe allrs587784231
SNP Nexus

SNPshotrs587784231
SNPdbers587784231
MSV3drs587784231
GWAS Ctlgrs587784231
Max Magnitude0
ClinVar
Risk rs587784231(;)
Alt rs587784231(;)
Reference rs587784231(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene OFD1
CLNDBN not provided
Reversed 0
HGVS NC_000023.10:g.13774807delA
CLNSRC
CLNACC RCV000146978.1,