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Variant (rsID / SNP)

rs3803736

QRICH2

rs3803736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to QRICH2. Location: chromosome 17, position 74,289,242. The table records no clinical significance for this variant.

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Reference-table entries

QRICH2Not classified
Variant type
synonymous_variant
Chromosome / position
17:74289242
HGVS
NM_001388453.1,c.1566A>G,p.Gln522Gln
Allele change
Synonymous_Q356Q

Public references

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