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Variant (rsID / SNP)

rs11559078

GTF3C3

rs11559078 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GTF3C3. Location: chromosome 2, position 197,662,526. The table records no clinical significance for this variant.

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Reference-table entries

GTF3C3Not classified
Variant type
missense_variant
Chromosome / position
2:197662526
HGVS
NM_012086.5,c.209A>G,p.Asn70Ser
Allele change
Missense_N70S

Public references

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