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Variant (rsID / SNP)

rs73996306

QRICH2

rs73996306 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to QRICH2. Location: chromosome 17, position 74,300,497. The table records no clinical significance for this variant.

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Reference-table entries

QRICH2Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
17:74300497
HGVS
NM_001388453.1,c.704C>T,p.Ala235Val
Allele change
Missense_A69V

Public references

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