Variant (rsID / SNP)

rs7516332

rs7516332 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PATJ. Location: chromosome 1, position 62,261,168. The table records no clinical significance for this variant.

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Reference-table entries

PATJNot classified

Variant type: missense_variant
Chromosome / position: 1:62261168
HGVS: NM_001350145.3,c.1198A>G,p.Ile400Val
Allele change: Missense_I400V

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.