Variant (rsID / SNP)

rs998532

rs998532 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TTF2. Location: chromosome 1, position 117,617,705. The table records no clinical significance for this variant.

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Reference-table entries

TTF2Not classified

Variant type: missense_variant
Chromosome / position: 1:117617705
HGVS: NM_003594.4,c.499A>G,p.Lys167Glu
Allele change: Missense_K167E

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.