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rs863223402

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs863223402(-;G)
Make rs863223402(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position83971880
GeneHNRNPK
is asnp
is mentioned by
dbSNPrs863223402
dbSNP (old)rs863223402
ClinGenrs863223402
ebirs863223402
HLIrs863223402
Exacrs863223402
Gnomadrs863223402
Varsomers863223402
Maprs863223402
PheGenIrs863223402
Biobankrs863223402
1000 genomesrs863223402
hgdprs863223402
ensemblrs863223402
gopubmedrs863223402
geneviewrs863223402
scholarrs863223402
googlers863223402
pharmgkbrs863223402
gwascentralrs863223402
openSNPrs863223402
23andMers863223402
23andMe allrs863223402
SNP Nexus

SNPshotrs863223402
SNPdbers863223402
MSV3drs863223402
GWAS Ctlgrs863223402
Max Magnitude0
ClinVar
Risk rs863223402(G;G)
Alt rs863223402(G;G)
Reference Rs863223402(-;-)
Significance Pathogenic
Disease AU-KLINE SYNDROME not provided
Variation info
Gene HNRNPK
CLNDBN AU-KLINE SYNDROME not provided
Reversed 1
HGVS NC_000009.11:g.86586796dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000195287.2, RCV000203300.1,