Variant (rsID / SNP)

rs2303929

rs2303929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC4A2. Location: chromosome 7, position 150,761,314. The table records no clinical significance for this variant.

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Reference-table entries

SLC4A2Not classified

Variant type: missense_variant
Chromosome / position: 7:150761314
HGVS: NM_001199692.3,c.77G>A,p.Gly26Glu
Allele change: Missense_G26E

Associated conditions / phenotypes

Primary Biliary Cholangitis|Biliary Cirrhosis, Primary, 1|Liver Cirrhosis

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.