Variant (rsID / SNP)

rs1898071

rs1898071 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LRMDA. Location: chromosome 10, position 77,807,027. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LRMDABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:77807027
Cytoband: 10q22.3
HGVS: NM_001305581.2(LRMDA):c.364T>C (p.Leu122=)
Allele change: Synonymous_L122L

Associated conditions / phenotypes

Oculocutaneous albinism type 7

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.