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Variant (rsID / SNP)

rs41304151

AHCTF1

rs41304151 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AHCTF1. Location: chromosome 1, position 247,024,326. The table records no clinical significance for this variant.

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Reference-table entries

AHCTF1Not classified
Variant type
missense_variant
Chromosome / position
1:247024326
HGVS
NM_015446.5,c.4034C>T,p.Thr1345Met
Allele change
Missense_T1336M

Public references

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