Variant (rsID / SNP)

rs1871892

rs1871892 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FNDC8, RAD51D. Location: chromosome 17, position 33,448,818. The table records no clinical significance for this variant.

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Reference-table entries

FNDC8Not classified

Variant type: missense_variant
Chromosome / position: 17:33448818
HGVS: NM_017559.4,c.106T>C,p.Ser36Pro
Allele change: Missense_S36P

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.