Variant (rsID / SNP)

rs11646443

rs11646443 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KCNG4. Location: chromosome 16, position 84,270,476. The table records no clinical significance for this variant.

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Reference-table entries

KCNG4Not classified

Variant type: missense_variant
Chromosome / position: 16:84270476
HGVS: NM_172347.3,c.616C>T,p.Arg206Trp
Allele change: Missense_R206W

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.