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Variant (rsID / SNP)

rs7904014

PTER

rs7904014 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PTER. Location: chromosome 10, position 16,547,058. The table records no clinical significance for this variant.

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Reference-table entries

PTERNot classified
Variant type
synonymous_variant
Chromosome / position
10:16547058
HGVS
NM_001001484.3,c.738A>G,p.Gln246Gln
Allele change
Synonymous_Q246Q

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.