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rs1057518237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs1057518237(-;ACCC)
Make rs1057518237(ACCC;ACCC)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position74685537
GeneHEXB
is asnp
is mentioned by
dbSNPrs1057518237
dbSNP (old)rs1057518237
ClinGenrs1057518237
ebirs1057518237
HLIrs1057518237
Exacrs1057518237
Gnomadrs1057518237
Varsomers1057518237
LitVarrs1057518237
Maprs1057518237
PheGenIrs1057518237
Biobankrs1057518237
1000 genomesrs1057518237
hgdprs1057518237
ensemblrs1057518237
gopubmedrs1057518237
geneviewrs1057518237
scholarrs1057518237
googlers1057518237
pharmgkbrs1057518237
gwascentralrs1057518237
openSNPrs1057518237
23andMers1057518237
23andMe allrs1057518237
SNPshotrs1057518237
SNPdbers1057518237
MSV3drs1057518237
GWAS Ctlgrs1057518237
Max Magnitude0
ClinVar
Risk rs1057518237(CACC;CACC)
Alt rs1057518237(CACC;CACC)
Reference Rs1057518237(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene HEXB
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.73981359_73981362dupACCC
CLNSRC
CLNACC RCV000414696.1,