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Variant (rsID / SNP)

rs347675

QRICH2

rs347675 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to QRICH2. Location: chromosome 17, position 74,275,160. The table records no clinical significance for this variant.

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Reference-table entries

QRICH2Not classified
Variant type
synonymous_variant
Chromosome / position
17:74275160
HGVS
NM_001388453.1,c.4878G>A,p.Thr1626Thr
Allele change
Synonymous_T1460T

Public references

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