Variant (rsID / SNP)

rs886090

rs886090 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SURF6. Location: chromosome 9, position 136,199,503. The table records no clinical significance for this variant.

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Reference-table entries

SURF6Not classified

Variant type: missense_variant
Chromosome / position: 9:136199503
HGVS: NM_006753.6,c.487C>T,p.Arg163Trp
Allele change: Synonymous_C162C

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.