Variant (rsID / SNP)

rs12963653

rs12963653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TAF4B. Location: chromosome 18, position 23,872,235. The table records no clinical significance for this variant.

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Reference-table entries

TAF4BNot classified

Variant type: missense_variant
Chromosome / position: 18:23872235
HGVS: NM_001293725.2,c.1631A>G,p.Asn544Ser
Allele change: Missense_N539S

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.