Variant (rsID / SNP)

rs147665041

rs147665041 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NID1. Location: chromosome 1, position 236,157,150. Clinical significance in the table: Uncertain significance.

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Reference-table entries

NID1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 1:236157150
Cytoband: 1q42.3
HGVS: NM_002508.3(NID1):c.2550G>C (p.Gln850His)
Allele change: Missense_Q850H

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.