Variant (rsID / SNP)

rs6657616

rs6657616 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CATSPER4. Location: chromosome 1, position 26,527,951. The table records no clinical significance for this variant.

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Reference-table entries

CATSPER4Not classified

Variant type: missense_variant
Chromosome / position: 1:26527951
HGVS: NM_198137.2,c.1306G>A,p.Asp436Asn
Allele change: Missense_D436N

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.