Variant (rsID / SNP)

rs1048886

rs1048886 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SDHAF4. Location: chromosome 6, position 71,289,189. The table records no clinical significance for this variant.

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Reference-table entries

SDHAF4Not classified

Variant type: missense_variant
Chromosome / position: 6:71289189
HGVS: NM_145267.3,c.137A>G,p.Gln46Arg
Allele change: Missense_Q46R

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.