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Variant (rsID / SNP)

rs34351170

PRKCSH

rs34351170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRKCSH. Location: chromosome 19, position 11,559,907. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

PRKCSHBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
19:11559907
Cytoband
19p13.2
HGVS
NM_001289104.2(PRKCSH):c.1378A>G (p.Ile460Val)
Allele change
Missense_I460V

Associated conditions / phenotypes

Polycystic liver disease 1

Public references

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