Variant (rsID / SNP)

rs147164392

rs147164392 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHD7. Location: chromosome 8, position 61,654,322. Clinical significance in the table: Uncertain significance.

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Reference-table entries

CHD7Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 8:61654322
Cytoband: 8q12.2
HGVS: NM_017780.4(CHD7):c.331C>T (p.Pro111Ser)
Allele change: Missense_P111S

Associated conditions / phenotypes

CHARGE association

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.