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Variant (rsID / SNP)

rs2072994

DISP3

rs2072994 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DISP3. Location: chromosome 1, position 11,579,470. The table records no clinical significance for this variant.

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Reference-table entries

DISP3Not classified
Variant type
missense_variant
Chromosome / position
1:11579470
HGVS
NM_020780.2,c.1948G>A,p.Ala650Thr
Allele change
Missense_A650T

Public references

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