Variant (rsID / SNP)

rs61741737

rs61741737 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to C12ORF71, C12orf71. Location: chromosome 12, position 27,234,914. The table records no clinical significance for this variant.

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Reference-table entries

C12ORF71Not classified

Variant type: missense_variant
Chromosome / position: 12:27234914
HGVS: NM_001080406.2,c.503C>T,p.Pro168Leu
Allele change: Missense_P168L

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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