Variant (rsID / SNP)

rs55729978

rs55729978 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ELF3. Location: chromosome 1, position 201,981,774. The table records no clinical significance for this variant.

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Reference-table entries

ELF3Not classified

Variant type: missense_variant
Chromosome / position: 1:201981774
HGVS: NM_001114309.2,c.485G>A,p.Gly162Asp
Allele change: Missense_G162D

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.