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Variant (rsID / SNP)

rs3743771

CHD9

rs3743771 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CHD9. Location: chromosome 16, position 53,358,439. The table records no clinical significance for this variant.

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Reference-table entries

CHD9Not classified
Variant type
missense_variant
Chromosome / position
16:53358439
HGVS
NM_001308319.2,c.8326A>G,p.Thr2776Ala
Allele change
Missense_T2760A

Associated conditions / phenotypes

Missense_T2254A

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.