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rs876657398

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876657398(A;C)
Make rs876657398(C;C)
ReferenceGRCh38.p2 38.2/147
Chromosome4
Position8868090
GeneHMX1
is asnp
is mentioned by
dbSNPrs876657398
ebirs876657398
HLIrs876657398
Exacrs876657398
Varsomers876657398
Maprs876657398
PheGenIrs876657398
hapmaprs876657398
1000 genomesrs876657398
hgdprs876657398
ensemblrs876657398
gopubmedrs876657398
geneviewrs876657398
scholarrs876657398
googlers876657398
pharmgkbrs876657398
gwascentralrs876657398
openSNPrs876657398
23andMers876657398
23andMe allrs876657398
SNP Nexus

SNPshotrs876657398
SNPdbers876657398
MSV3drs876657398
GWAS Ctlgrs876657398
Max Magnitude0
ClinVar
Risk rs876657398(C;C)
Alt rs876657398(C;C)
Reference rs876657398(A;A)
Significance Pathogenic
Disease Oculoauricular syndrome
Variation info
Gene HMX1
CLNDBN Oculoauricular syndrome
Reversed 1
HGVS NC_000004.11:g.8869816T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000172907.2,