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rs772570880

From SNPedia

Orientationplus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs772570880(-;-)
Make rs772570880(-;CT)
ReferenceGRCh38.p2 38.2/147
Chromosome5
Position138566715
GeneHSPA9, LOC105379193
is asnp
is mentioned by
dbSNPrs772570880
ebirs772570880
HLIrs772570880
Exacrs772570880
Varsomers772570880
Maprs772570880
PheGenIrs772570880
hapmaprs772570880
1000 genomesrs772570880
hgdprs772570880
ensemblrs772570880
gopubmedrs772570880
geneviewrs772570880
scholarrs772570880
googlers772570880
pharmgkbrs772570880
gwascentralrs772570880
openSNPrs772570880
23andMers772570880
23andMe allrs772570880
SNP Nexus

SNPshotrs772570880
SNPdbers772570880
MSV3drs772570880
GWAS Ctlgrs772570880
Max Magnitude0
ClinVar
Risk rs772570880(;)
Alt rs772570880(;)
Reference rs772570880(CT;CT)
Significance Pathogenic
Disease Even-plus syndrome
Variation info
Gene HSPA9
CLNDBN Even-plus syndrome
Reversed 0
HGVS NC_000005.9:g.137902404_137902405delCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000209995.2,