Variant (rsID / SNP)

rs4339048

rs4339048 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BAIAP2L2. Location: chromosome 22, position 38,495,011. The table records no clinical significance for this variant.

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Reference-table entries

BAIAP2L2Not classified

Variant type: intron_variant
Chromosome / position: 22:38495011
HGVS: NM_025045.6,c.277-522A>G
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.