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Variant (rsID / SNP)

rs6501880

QRICH2

rs6501880 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to QRICH2. Location: chromosome 17, position 74,289,705. The table records no clinical significance for this variant.

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Reference-table entries

QRICH2Not classified
Variant type
missense_variant
Chromosome / position
17:74289705
HGVS
NM_001388453.1,c.1103T>C,p.Leu368Ser
Allele change
Missense_L202S

Public references

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