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rs763817505

From SNPedia

Orientationplus
Geno Mag Summary
(AT;AT) 0 common in clinvar
Make rs763817505(-;-)
Make rs763817505(-;AT)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position138570960
GeneHSPA9, LOC105379193
is asnp
is mentioned by
dbSNPrs763817505
ebirs763817505
HLIrs763817505
Exacrs763817505
Varsomers763817505
Maprs763817505
PheGenIrs763817505
hapmaprs763817505
1000 genomesrs763817505
hgdprs763817505
ensemblrs763817505
gopubmedrs763817505
geneviewrs763817505
scholarrs763817505
googlers763817505
pharmgkbrs763817505
gwascentralrs763817505
openSNPrs763817505
23andMers763817505
23andMe allrs763817505
SNP Nexus

SNPshotrs763817505
SNPdbers763817505
MSV3drs763817505
GWAS Ctlgrs763817505
Max Magnitude0
ClinVar
Risk
Alt
Reference Rs763817505(AT;AT)
Significance Pathogenic
Disease Anemia
Variation info
Gene HSPA9
CLNDBN Anemia, sideroblastic, 4
Reversed 0
HGVS NC_000005.9:g.137906649_137906650delAT
CLNSRC OMIM Allelic Variant
CLNACC RCV000209839.2,