Variant (rsID / SNP)

rs1136001

rs1136001 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NTAN1, PDXDC1. Location: chromosome 16, position 15,131,974. The table records no clinical significance for this variant.

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Reference-table entries

NTAN1Not classified

Variant type: missense_variant
Chromosome / position: 16:15131974
HGVS: NM_173474.4,c.847C>A,p.His283Asn
Allele change: Silent

Associated conditions / phenotypes

Missense_H178N

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.