Variant (rsID / SNP)

rs13362048

rs13362048 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABLIM3. Location: chromosome 5, position 148,578,636. The table records no clinical significance for this variant.

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Reference-table entries

ABLIM3Not classified

Variant type: intron_variant
Chromosome / position: 5:148578636
HGVS: NM_001301015.3,c.335+671T>C
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.