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rs869312659

From SNPedia

Orientationminus
Geno Mag Summary
(TTAATA;TTAATA) 0 common in clinvar
Make rs869312659(-;-)
Make rs869312659(-;TTAATA)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position138559896
GeneHSPA9, LOC105379193
is asnp
is mentioned by
dbSNPrs869312659
ebirs869312659
HLIrs869312659
Exacrs869312659
Varsomers869312659
Maprs869312659
PheGenIrs869312659
hapmaprs869312659
1000 genomesrs869312659
hgdprs869312659
ensemblrs869312659
gopubmedrs869312659
geneviewrs869312659
scholarrs869312659
googlers869312659
pharmgkbrs869312659
gwascentralrs869312659
openSNPrs869312659
23andMers869312659
23andMe allrs869312659
SNP Nexus

SNPshotrs869312659
SNPdbers869312659
MSV3drs869312659
GWAS Ctlgrs869312659
Max Magnitude0
ClinVar
Risk rs869312659(;)
Alt rs869312659(;)
Reference rs869312659(TTAATA;TTAATA)
Significance Pathogenic
Disease Anemia
Variation info
Gene HSPA9
CLNDBN Anemia, sideroblastic, 4
Reversed 1
HGVS NC_000005.9:g.137895585_137895590delTATTAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000209862.2,