Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs8207

PPIG

rs8207 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPIG. Location: chromosome 2, position 170,493,863. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

PPIGNot classified
Variant type
missense_variant
Chromosome / position
2:170493863
HGVS
NM_004792.3,c.2095A>G,p.Asn699Asp
Allele change
Missense_N699D

Public references

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