Variant (rsID / SNP)

rs78052401

rs78052401 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C4ORF45, C4orf45. Location: chromosome 4, position 159,836,336. The table records no clinical significance for this variant.

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Reference-table entries

C4ORF45Not classified

Variant type: missense_variant
Chromosome / position: 4:159836336
HGVS: NM_152543.3,c.532C>T,p.Pro178Ser
Allele change: Missense_P178S

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.