Variant (rsID / SNP)

rs79937396

rs79937396 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIPA1L1. Location: chromosome 14, position 72,169,130. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SIPA1L1Not classified

Variant type: missense_variant
Chromosome / position: 14:72169130
HGVS: NM_001354285.2,c.3554T>C,p.Ile1185Thr
Allele change: Missense_I1185T

Associated conditions / phenotypes

Missense_I1185T|Missense_I691T|Missense_I1185T|Missense_I1185T

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.