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rs879255263

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs879255263(-;-)
Make rs879255263(-;TT)
Make rs879255263(TT;TT)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position83971903
GeneHNRNPK
is asnp
is mentioned by
dbSNPrs879255263
ebirs879255263
HLIrs879255263
Exacrs879255263
Varsomers879255263
Maprs879255263
PheGenIrs879255263
hapmaprs879255263
1000 genomesrs879255263
hgdprs879255263
ensemblrs879255263
gopubmedrs879255263
geneviewrs879255263
scholarrs879255263
googlers879255263
pharmgkbrs879255263
gwascentralrs879255263
openSNPrs879255263
23andMers879255263
23andMe allrs879255263
SNP Nexus

SNPshotrs879255263
SNPdbers879255263
MSV3drs879255263
GWAS Ctlgrs879255263
Max Magnitude0
ClinVar
Risk rs879255263(TT;TT)
Alt rs879255263(TT;TT)
Reference rs879255263(;)
Significance Pathogenic
Disease AU-KLINE SYNDROME
Variation info
Gene HNRNPK
CLNDBN AU-KLINE SYNDROME
Reversed 1
HGVS NC_000009.11:g.86586818_86586819insAA
CLNSRC
CLNACC RCV000239391.1,