Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs61729862

PIP5K1A

rs61729862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIP5K1A. Location: chromosome 1, position 151,215,011. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

PIP5K1ANot classified
Variant type
synonymous_variant
Chromosome / position
1:151215011
HGVS
NM_001135638.2,c.1608A>G,p.Leu536Leu
Allele change
Synonymous_L524L

Public references

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