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rs863223403

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863223403(A;A)
Make rs863223403(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome9
Position83975462
GeneHNRNPK
is asnp
is mentioned by
dbSNPrs863223403
ebirs863223403
HLIrs863223403
Exacrs863223403
Varsomers863223403
Maprs863223403
PheGenIrs863223403
hapmaprs863223403
1000 genomesrs863223403
hgdprs863223403
ensemblrs863223403
gopubmedrs863223403
geneviewrs863223403
scholarrs863223403
googlers863223403
pharmgkbrs863223403
gwascentralrs863223403
openSNPrs863223403
23andMers863223403
23andMe allrs863223403
SNP Nexus

SNPshotrs863223403
SNPdbers863223403
MSV3drs863223403
GWAS Ctlgrs863223403
Max Magnitude0
ClinVar
Risk rs863223403(A;A)
Alt rs863223403(A;A)
Reference rs863223403(G;G)
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.86590377C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000195291.3, RCV000203308.1,