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rs869312922

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs869312922(G;T)
Make rs869312922(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position19197622
GeneRFXANK
is asnp
is mentioned by
dbSNPrs869312922
ebirs869312922
HLIrs869312922
Exacrs869312922
Varsomers869312922
Maprs869312922
PheGenIrs869312922
hapmaprs869312922
1000 genomesrs869312922
hgdprs869312922
ensemblrs869312922
gopubmedrs869312922
geneviewrs869312922
scholarrs869312922
googlers869312922
pharmgkbrs869312922
gwascentralrs869312922
openSNPrs869312922
23andMers869312922
23andMe allrs869312922
SNP Nexus

SNPshotrs869312922
SNPdbers869312922
MSV3drs869312922
GWAS Ctlgrs869312922
Max Magnitude0
ClinVar
Risk rs869312922(T;T)
Alt rs869312922(T;T)
Reference rs869312922(G;G)
Significance Pathogenic
Disease Inborn genetic diseases
Variation info
Gene RFXANK
CLNDBN Inborn genetic diseases
Reversed 0
HGVS NC_000019.9:g.19308431G>T
CLNSRC
CLNACC RCV000210620.1,