Variant (rsID / SNP)

rs12910925

rs12910925 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GABRA5. Location: chromosome 15, position 27,184,435. The table records no clinical significance for this variant.

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Reference-table entries

GABRA5Not classified

Variant type: intron_variant
Chromosome / position: 15:27184435
HGVS: NM_000810.4,c.725-637C>T
Allele change: Silent

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.