Variant (rsID / SNP)

rs6998760

rs6998760 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PSKH2. Location: chromosome 8, position 87,076,520. The table records no clinical significance for this variant.

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Reference-table entries

PSKH2Not classified

Variant type: missense_variant
Chromosome / position: 8:87076520
HGVS: NM_033126.3,c.526G>T,p.Ala176Ser
Allele change: Missense_A176S

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.