Variant (rsID / SNP)

rs117698926

rs117698926 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to MTPAP. Location: chromosome 10, position 30,605,044. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

MTPAPBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 10:30605044
Cytoband: 10p11.23
HGVS: NM_018109.4(MTPAP):c.1312+3A>G
Allele change: Silent

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.