Variant (rsID / SNP)

rs138635992

rs138635992 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHD1. Location: chromosome 5, position 98,192,165. The table records no clinical significance for this variant.

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Reference-table entries

CHD1Not classified

Variant type: conservative_inframe_deletion
Chromosome / position: 5:98192165
HGVS: NM_001364113.3,c.5314_5316delCCT,p.Pro1772del

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.