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Variant (rsID / SNP)

rs760644

PRRC2C

rs760644 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRRC2C. Location: chromosome 1, position 171,509,327. The table records no clinical significance for this variant.

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Reference-table entries

PRRC2CNot classified
Variant type
missense_variant
Chromosome / position
1:171509327
HGVS
NM_001387844.1,c.2722G>A,p.Ala908Thr
Allele change
Missense_A906T

Public references

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