Variant (rsID / SNP)

rs7850542

rs7850542 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SPATA31E1. Location: chromosome 9, position 90,500,405. The table records no clinical significance for this variant.

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Reference-table entries

SPATA31E1Not classified

Variant type: missense_variant
Chromosome / position: 9:90500405
HGVS: NM_178828.5,c.1003A>C,p.Thr335Pro
Allele change: Silent

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.