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Variant (rsID / SNP)

rs6722682

GCFC2

rs6722682 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GCFC2. Location: chromosome 2, position 75,907,351. The table records no clinical significance for this variant.

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Reference-table entries

GCFC2Not classified
Variant type
missense_variant
Chromosome / position
2:75907351
HGVS
NM_003203.5,c.1780A>G,p.Thr594Ala
Allele change
Missense_T425A

Public references

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