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rs797044889

From SNPedia

Orientationminus
Make rs797044889(-;-)
Make rs797044889(-;CG)
ReferenceGRCh38.p2 38.2/147
ChromosomeX
Position53250523
GeneIQSEC2
is asnp
is mentioned by
dbSNPrs797044889
ClinGenrs797044889
ebirs797044889
HLIrs797044889
Exacrs797044889
Varsomers797044889
Maprs797044889
PheGenIrs797044889
hapmaprs797044889
1000 genomesrs797044889
hgdprs797044889
ensemblrs797044889
gopubmedrs797044889
geneviewrs797044889
scholarrs797044889
googlers797044889
pharmgkbrs797044889
gwascentralrs797044889
openSNPrs797044889
23andMers797044889
23andMe allrs797044889
SNP Nexus

SNPshotrs797044889
SNPdbers797044889
MSV3drs797044889
GWAS Ctlgrs797044889
Max Magnitude
ClinVar
Risk
Alt
Reference Rs797044889(CG;CG)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene IQSEC2
CLNDBN Inborn genetic diseases
Reversed 1
HGVS NC_000023.10:g.53279705_53279706delCG
CLNSRC
CLNACC RCV000190711.1,