RS696217 GHRL

Health Risk Chr 3:10289772 snv missense variant
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:GHRELIN
Associated Conditions
Population Frequencies
gnomAD ALL
91.7%
1kG AFR
99.1%
1kG ALL
91.7%
1kG AMR
4.8%
1kG EAS
19.1%
1kG EUR
91.3%
1kG SAS
9.3%
Other Variants in GHRL
Ask Dr. Hemsworth about this variant